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<h3>Job Description</h3>
Join a global community of talented professionals to shape the future of AI. Earn up to $15 USD/hr and additional rewards based on quality of submission.
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Outlier is committed to improving the intelligence &amp; safety of AI models. Owned and operated by Scale AI, we’ve recently been featured in Forbes for partnering experts with top AI labs to provide the high quality data for LLMs. We believe AI can only perform as well as the data it’s trained on. That’s why we work with contributors from all over the world, who help improve AI models by providing expert human feedback. This data has led to AI advancements for the world's leading AI labs and large language model builders. We’ve built a best-in-class remote work platform for our freelance contributors to provide valuable, specialized skills, and we in turn strive to provide them with a positive experience based on our core pillars of reliability, transparency, and flexibility.
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What you will be doing
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We are looking for someone who speaks fluent English to contribute their expertise toward training and refining cutting-edge AI systems.
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<ul>\n
<li>Adopt a “user mindset” to produce natural data to meet the realistic needs you have or would use AI for.</li>
\n
<li>Use the tool of rubrics to address user needs in a structured way.</li>
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<li>Evaluate AI outputs by reviewing and ranking reasoning and problem-solving responses from large language models.</li>
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<li>Contribute across projects depending on your specific skillset and experience.</li>
\n</ul>
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What we’re looking for
\n
<ul>\n
<li>Education: Bachelor’s degree or higher (or currently enrolled).</li>
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<li>Analytical and Problem-Solving Skills: Ability to develop complex, professional-level prompts and evaluate nuanced AI reasoning.</li>
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<li>Strong Writing: Clear, concise, and engaging writing to explain decisions or critique responses.</li>
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<li>Attention to Detail: Commitment to accuracy and ability to assess technical aspects of model outputs. Nice to Haves:</li>
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<li>Experience in fields like literature, creative writing, history, philosophy, theology, etc.</li>
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<li>Prior writing or editorial experience (content strategist, technical writer, editor, etc.).</li>
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<li>Interest or background in AI, machine learning, or creative tech tools.</li>
\n</ul>
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Compensation and benefits
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Earn up to $15 USD/hr, paid out weekly
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Rates vary based on quality, accuracy, and time spent. Paid via PayPal &amp; AirTM
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Free access to Model Playground
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Interact, experiment and engage with leading large language models free of cost
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Flexible schedule and time commitment
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No contracts, no 9-to-5. You control your schedule. (Most experts spend 5-10 hours/week, up to 40 hours working from home
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Join a global community of Coding experts
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Join a global network of experts contributing to advanced AI tools
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Disclaimer: For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.
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Equal Opportunity Employer: Outlier is committed to fostering a diverse and inclusive work environment. We welcome applicants from all backgrounds and celebrate diversity in our workforce.

Research Analyst AI Content (Remote)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
The Senior Scientist ensures study design; execution and reporting align with regulatory and client project specifications. The Senior Scientist provides critical client consultation throughout study life cycle and ensures lab compliance to study design. This role will support Electrophysiology projects including cardiac safety screening in a GLP-compliant electrophysiology lab and serve as a Principal Investigator for regulated studies. This role requires technical expertise, portfolio leadership, leadership competencies, and proficiency in client communication within a contract research organization.
Senior Scientist — Regulatory Cardiac Safety/Electrophysiology (Scientist II) responsibilities include, but are not limited to, the following:
The Senior Scientist is a scientific leadership position, responsible for providing guidance and alignment between our customer base, the industry at large, commercial teams and service operations. This role is a hands-on laboratory-based role and will be collaborative and influential in a broad network of business functions in support of delivering high quality services to our valued customers, and driving business growth, brand recognition, and alignment with Eurofins core competencies. This position will train and mentor junior staff, responsible to take informed decision to move projects ahead, set direction, champion change and directly contribute to achieving departments goals and strategies.
<ul>
<li>Develops client and stakeholder relationships through technical leadership and collaboration</li>
<li>Manages client projects in all phases of study life cycle from study design to reporting</li>
<li>Provides guidance and oversight for compliance and scientific integrity of the studies to ensure that studies are performed in a compliant manner</li>
<li>Understands and follows all procedures and processes required for work performed under Regulatory Compliance (i.e. GxP, FDA/GLP and GCP, OECD, CLIA, etc.) and completes annual GLP training</li>
<li>Directs investigations of service operations, such as deviation reports, non-conforming reports, corrective action reports, etc. Produces documentation according to established standards</li>
<li>Drafts and approves operations documents to assure consistency with regulatory standards and requirements. (I.e. SOPs, batch records, training records, etc.)</li>
<li>Responsible for data generation, review, analysis review and ensuring accuracy and integrity of reporting</li>
<li>Provides scientific guidance that supports technical writing and final review of Validation Plans and Reports as required</li>
<li>Supports client services team in generating proposals, RFPs, study plans and scope of work preparation. Assists pricing team in completing custom pricing and cost analysis</li>
<li>Completes required training and supports 100% of Employee Health and Safety requirements</li>
<li>Manages responsible use of confidential IT and business systems, as required</li>
<li>Ensures accurate data management and reporting, with the highest integrity, and manages quality control on project data and reports</li>
<li>Accountable for delivering to unit and site key performance metrics (quality, delivery on time)</li>
<li>Supports site goals and demonstrates Eurofins' competencies, as defined in the job plan</li>
<li>Provides training to colleagues and external end users, when required</li>
<li>Performs other duties, as assigned</li>
</ul>
Qualifications 
Basic Minimum Education Qualifications:
<ul>
<li>
M.A. or M.S. with minimum 5 years relevant experience
</li>
</ul>
OR
<ul>
<li>
Ph.D. with minimum 3 years relevant experience
</li>
</ul>
Basic Minimum Qualifications:
<ul>
<li>Demonstrated experience in manual patch clamp electrophysiology in a GLP-compliant laboratory is a plus.</li>
<li>Scientific expertise in Ion Channel electrophysiology and applications to execute safety pre-clinical studies.</li>
<li>Technical experience and knowledge in supporting compound cardiac safety profiling within drug discovery programs, from early drug discovery to IND submission life cycle.</li>
<li>Experience developing client relationships, supporting technical correspondence, drafting and presenting scientific proposals to clients.</li>
<li>Experience in drafting and executing equipment and method validation according to 21CFR11 compliance.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.&nbsp;</li>
</ul>
The Ideal Candidate Possesses the Following:
<ul>
<li>Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health.</li>
<li>Excellent interpersonal, verbal and written skills, including ability to prepare detailed scientific reports and group presentations.</li>
<li>Demonstrates a working understanding of international regulatory requirements and aptitude to stay relevant on topical scientific publications.</li>
<li>Ability to support project management, plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources.</li>
<li>Demonstrated experience in working effectively with lab operations, business development, marketing, and outsourcing stakeholders.</li>
<li>Experience with leading and influencing cross-functional teams effectively</li>
</ul>
 Additional Information 
Position is full-time,&nbsp;with overtime as needed. Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply.
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Scientist -- Regulatory Cardiac Safety/Electrophysiology (Scientist II)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Members of the Metrology team support processes for laboratories at Viracor with a focus on maintaining CLIA, CAP and NYDOH, GxP accreditation by using and maintaining procedures and software or other methods to perform, train, document, assist others to ensure complete and appropriate documentation of required tasks and records. The Laboratory Metrology Technician (Tech) is responsible for conducting and documenting cleaning, calibration, preventive maintenance functions, and documenting excursions from expected performance as outlined by management in the laboratory areas.
Laboratory Metrology Technician&nbsp;responsibilities include, but are not limited to, the following:
Level I –
<ul>
<li>Perform and/or assist with instrument maintenance such as plate readers and washers, liquid handling equipment, front end lab automation equipment, centrifuges, balances, etc.</li>
<li>Responsible for performing and documenting cleaning of the laboratory areas and equipment</li>
<li>Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.</li>
<li>Maintain cleaning and maintenance records as required</li>
<li>Instrument calibration activities and documentation including environmental monitoring system and laboratory equipment as directed (Pipettes/Temperature probes)</li>
<li>Respond to and document environmental alerts, ensuring documentation of actions taken/escalate as needed</li>
<li>Instrument power cycles/UPS maintenance as required</li>
<li>Inventory management and upkeep of pipettes including supplying backups and replacements as requested</li>
<li>Maintain proper records in equipment tracking software by documenting actions and maintaining schedule of required activities</li>
<li>Administration duties within the department and investigation activities which includes providing documentation as requested by internal or external auditors</li>
<li>Obtain and maintain proficiency in software programs or tools used in department</li>
<li>Support development of system and process improvements that would enhance compliance to requirements</li>
<li>Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies</li>
<li>Adhere to policies and protocols in the laboratory</li>
<li>Work closely and communicate with other laboratory associates to complete daily activities efficiently</li>
<li>Represent department and the organization favorably and in accordance with established company standards and associate attributes at all times</li>
<li>Other duties as assigned by management</li>
</ul>
Level II –
Fully meets the responsibilities of Level I plus the following:
<ul>
<li>Highly proficient in multiple processes managed by the department</li>
<li>Able to train, assist users or clients with questions and/or issues, participate in validation of updates</li>
<li>Provide training and orientation of testing personnel as directed (pipettes and environmental monitoring)</li>
<li>Maintenance of Laboratory equipment schedules, including management of calibration/maintenance tracking program/software, temperature monitoring system, and pipette calibration program, ensuring that calibrations are correct and current.</li>
<li>Understand and demonstrate proficiency with quality monitoring activities such as quality indicators and quality reporting related to equipment and monitoring such as KPIs for Quality Meeting</li>
<li>Communicates Metrology area needs to Facilities, Testing and Manufacturing personnel</li>
<li>Contacts suppliers/vendors as required</li>
<li>Participate in data reporting, internal or external client reports as requested, using Excel or other software utilized for reporting, trending, and tracking</li>
<li>Participate in continual quality improvement projects company-wide</li>
<li>Participate in creation/revision of SOPs and training materials for the department as required and ensure policies and procedures are monitored and updated to include regulatory changes</li>
<li>Other duties as assigned by managemen</li>
</ul>
Qualifications 
Basic Minimum Education Qualifications:
<ul>
<li>Level I: GED or High school Diploma</li>
<li>Level II: BA/BS in biological, physical, chemical or clinical laboratory science preferred.</li>
</ul>
Basic Minimum Qualifications:
<ul>
<li>Level II: minimum of 2 years’ experience in a regulated laboratory (CAP/CLIA and/or GxP), as Laboratory Quality Tech I, or similar experience in Laboratory process ownership, e.g. laboratory technical roles.</li>
<li>Knowledge of the clinical laboratory environment preferred, including basic terminology, protocols and practices</li>
<li>Ability to initiate tasks and work efficiently with minimal supervision</li>
<li>Comfortable working in a laboratory setting</li>
<li>Knowledge of basic computer programs such as Microsoft Excel and Word including common applications in laboratory use</li>
<li>Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices</li>
<li>Position may require working hours outside of the normal work schedule when necessary</li>
<li>Ability to keep sensitive information confidential</li>
<li>Working knowledge of good laboratory practices and laboratory test methodologies.</li>
<li>Ability to identify aberrant data and potential quality/compliance concerns escalating to management.</li>
<li>Familiarity with six sigma scoring as applied to metrics/KPIs for quality</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
The Ideal Candidates Possesses the Following:
<ul>
<li>Ability to work both independently and as part of an integrated quality team</li>
<li>Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills</li>
<li>Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required</li>
<li>Ability to work both independently and as part of an integrated quality team</li>
<li>Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills</li>
<li>Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required</li>
<li>Ability to work proactively in a self-directed manner, taking initiative as required</li>
<li>Ability to make sound decisions with little or no supervision, including generating test data, performing analysis, and escalating when appropriate</li>
</ul>
Physical Requirements:
<ul>
<li>Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead</li>
<li>Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting</li>
<li>Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours)</li>
<li>Ability to lift and move items weighing up to 50 pounds</li>
<li>Using assistance as available, must have physical ability to push/pull heavy loads (may be in excess of 100 pounds</li>
<li>Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation</li>
<li>Ability to continuously operate a personal computer for extended periods of time (4 or more hours)</li>
<li>Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions</li>
</ul>
 Additional Information 
Position is part-time, working Thursday-Saturday: 7:00 pm - 11:00 pm and Sunday 3:00 pm -11:30 pm,&nbsp;with overtime as needed. Candidates currently living within a commutable distance of Lenexa, KS are encouraged to apply.
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Metrology Technician (Part-Time)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
<ul>
<li>Perform analytical test methods including HPLC in the GMP environment</li>
<li>Document laboratory work in notebooks/e-notebooks/logbooks/electronic systems. perform data integrity checks, data verification reviews, and communicate results through electronic systems</li>
<li>Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements</li>
<li>Coordinate workflow and perform daily monitoring to meet TAT</li>
<li>Prepare and review job plans, conduct semiannual performance reviews, keep training records up to date for assigned employees, perform succession planning in preparation for growth</li>
<li>Collaborate closely with leaders and clients in implementing overall business directives</li>
</ul>
Qualifications 
<ul>
<li>Experience with HPLC a minimum of 1 year of industry lab.</li>
<li>GMP quality system and lab operations experience</li>
<li>&nbsp;Excellent communication (oral and written) and attention to detail</li>
<li>&nbsp;Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and&nbsp;a&nbsp;positive attitude</li>
<li>Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies</li>
<li>Bachelor's degree in biology, chemistry, or other related degree concentration, or&nbsp;equivalent directly related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to work independently and as part of a team, and possess self-motivation, adaptability, and a positive attitude</li>
<li>Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment</li>
<li>Strong focus on quality, teamwork, and productivity</li>
<li>Proactive, positive, solution-oriented leadership style with ability to prioritize and coordinate simultaneous projects with varying deadlines</li>
<li>Strength in employee engagement, morale, and retention&nbsp;</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, Monday - Friday&nbsp;8am to 5 pm</li>
<li>Ability to work overtime as required.</li>
<li>Tasks require repetitive motion and standing for long periods of time.</li>
<li>May be required to respond to off-shift operational issues.</li>
<li>Candidates currently living within a commutable distance of Indianapolis, IN&nbsp;are encouraged to apply.</li>
<li>Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Chemist- Group Leader

<h3>Job Description</h3>
Job Description
About Us
Sigmatech is a trusted provider of high-quality technical and professional services to government and commercial customers. With a strong focus on innovation, integrity, and excellence, we support our clients with the tools, talent, and technology they need to succeed.
A successful candidate will be responsible for the following:
<ul>
<li>Strategic Analysis: Develop study plans for complex problems with minimal precedent</li>
<li>Data Analysis: Collect, organize, and analyze information from multiple sources including databases, surveys, and stakeholder feedback</li>
<li>Modeling: Build and manipulate mathematical models representing processes, systems, and operations</li>
<li>Decision Support: Provide analytical recommendations to senior leaders (O6-GO/SES level)</li>
<li>Innovation: Generate new study ideas and analytical approaches</li>
<li>Briefing: Present complex analytical findings to senior Army leadership</li>
<li>Collaboration: Work with cross-functional teams and coordinate with other Army Staff elements</li>
</ul>
This position is contingent upon contract award. Regular CONUS/OCONUS travel is required.
 
<ul>
<li>Bachelor's Degree in one of the following: Operations Research, Applied Mathematics, Statistics, Engineering (Systems or Industrial), or Computer Science. </li>
<li>Minimum 5 years of Operations Research Systems Analysis experience at senior military levels (HQDA, MACOMs, Army Service Component Commands, or equivalent Joint Service levels) </li>
<li>Required Technical Skills: </li>
</ul>
Software Proficiency:
<ul>
<ul>
<li>SAS (required for modeling and analysis)</li>
<li>Business Intelligence Tools (Qlik, Tableau)</li>
<li>Microsoft Office Suite (advanced Excel capabilities)</li>
<li>Statistical analysis software (R programming preferred)</li>
</ul>
</ul>
Analytical Techniques:
<ul>
<ul>
<li>ANOVA, Multiple Regression analysis</li>
<li>Forecasting and measurement analysis</li>
<li>Flow modeling and linear programming</li>
<li>Queuing theory and simulations</li>
<li>Cost-benefit analysis</li>
<li>Business reengineering/IDEF modeling</li>
</ul>
</ul>
<ul>
<li>Technical Expertise</li>
<ul>
<li>Advanced mathematical and statistical modeling</li>
<li>Linear and non-linear programming</li>
<li>Simulation and predictive modeling</li>
<li>Optimization techniques</li>
<li>Risk analysis and management</li>
<li>Capital investment analysis</li>
<li>Decision analysis supporting business units</li>
</ul>
<li>Ability to solve real-world problems in capital investment and system design</li>
<li>Demonstrated capability to brief and communicate complex analytical concepts to senior leadership</li>
<li>Experience with survey design and data interpretation</li>
<li>Proven track record in developing practical solutions to business problems through quantitative analysis</li>
</ul>
What We Offer
<ul>
<li>Competitive starting salary and a comprehensive benefits package including:</li>
<ul>
<li>Medical, Dental, and Vision insurance</li>
<li>401(k) with company match</li>
<li>Paid Time Off and holidays</li>
<li>Professional development and training opportunities</li>
</ul>
</ul>
Apply Today If you're ready to launch your career in the defense sector with a company that values excellence and growth, we'd love to hear from you. Apply now and become a part of the Sigmatech Team
 
EEO employer, including veterans and individuals with disabilities.

Senior Operations Research Analyst

<h3>Job Description</h3>
Job DescriptionDescriptionSenior Research Analyst WHO WE ARE: STAHL Companies provides the Program Management for its Channel of Commercial Technology companies in Government that consist of Small Businesses and New Technology start-ups. STAHL advocates for policies that can improve government services and maintain our government's competitive advantage, by bringing more technology into government programs. STAHL Companies advocates on behalf of our nation's innovative, new technology and small businesses looking to work with the U.S. government. We do this by aligning the voice of our small business members with advocacy for change in federal policy that will make the government market more accessible to small businesses and the commercial technology ecosystem. The Channel's founding Technical Board Members include former government leaders and IT executives passionate about bringing best-of-breed technology to the government. We are seeking a skilled and experienced Senior Research Analyst to join our team! Successful Stahl Companies employees possess the following traits: An ability to get things done: You are persistent, resourceful, results-oriented, and action-oriented. You constantly plan ahead and foresee issues before they occur. Analytical: In order to improve your comprehension of the market and the demands and problems of your clients, you have good analytical abilities and are at ease reading quantitative data. Creative mind-set: You are able to solve problems creatively and swiftly adjust. You possess a thorough understanding of product management principles and the ability to apply them when analysing data and making recommendations. Emotional Intelligence: You have a strong sense of self and excellent perception of how important relationships function. You are upbeat, sympathetic, adaptable, and inquisitive. Your genuineness, warmth, and competence help you win the respect of your co-workers. Trustworthy: You have a strong sense of morality, principles, and purpose. You are trustworthy because of how you conduct yourself. You are a living example of the company's values. Responsibilities:·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyze ONR Programs and individual project data in relationship to other internal and external parameters and data. Provide ONR with recommendations and responses to analyses findings. Examples include:·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyzing projects against external S&amp;T demand signals and recommending adjustments to maximize DON benefits.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyzing completed projects, their results, and final disposition.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting the development and reporting of S&amp;T Portfolio investment analyses.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Coordinating with the ONR PIIM Team on portfolio dashboard development and analysis.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Monitoring external S&amp;T efforts and analyzing their relationships to ONR programs. Developing recommendations for ONR management to coordinate with external S&amp;T investment. Examples include:·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Monitoring DARPA projects and supporting ONR participation in DARPA reviews.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Preparing S&amp;T roadmaps.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Monitoring Corporate OSD Prototyping and Concept Exploration programs (e.g. Joint Capability Technology·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Demonstration; Advancement of Science and Technology Priorities; Community of Interest Seedlings) to determine potential ONR benefit and courses of action.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting the DASN (RDT&amp;E) chartered Proposal Development Team.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting ONR interactions with the USD(R&amp;E) and Senior DoD Leadership.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting ONR participation in the OUSD(R&amp;E) Deputies’ Action Group.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Provide operational and technical expertise, and administrative support to ONR sub-portfolio directors.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Manage the oversight of ONR funded Unmanned Aircraft operations.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyze external documents and recommend ONR courses of action and response.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Answer specific questions and inquiries about the ONR Programs and their relationships.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Bin, categorize, and analyze ONR 03 S&amp;T projects for trend analysis, portfolio understanding, and compiled aggregate results.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Prepare briefs and reports with results of analyses. Qualifications:Requires a Master’s degree in science or engineering from an accredited college or university or Graduate-level professional military education (PME) in a technical or science curriculum and at least 15 years of experience in a related S&amp;T discipline. Experience with technology development and military requirements, systems, and operations is required. A minimum of 5-years of specific S&amp;T technical experience in the management support, planning and execution of technology transition programs is required. The candidate must have experience assembling, analyzing, and succinctly presenting information, conclusions and recommendations. Desired qualifications: Knowledge and experience in the primary ONR 03 Program the individual is proposed to support. Experience in conducting technology search, analysis, and road mapping. A master’s degree in science or engineering from an accredited college or university is preferred over a Graduate-level professional military education (PME) in a technical or science curriculum. *Position is contingent upon award. Work Location: Quantico, Virginia, United States MCWL &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Arlington, Virginia, United States ONR HQ To know more about the company, visit Stahl Companies (<a href="http://www.stahlusa.us" target="_blank">www.stahlusa.us</a>) or G4i Staffing Home (govg4inc.com) Key Responsibilities&nbsp;Analyze ONR Programs and individual project data in relationship to other internal and external parameters and data. Provide ONR with recommendations and responses to analyses findings. Examples include:·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyzing projects against external S&amp;T demand signals and recommending adjustments to maximize DON benefits.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyzing completed projects, their results, and final disposition.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting the development and reporting of S&amp;T Portfolio investment analyses.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Coordinating with the ONR PIIM Team on portfolio dashboard development and analysis.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Monitoring external S&amp;T efforts and analyzing their relationships to ONR programs. Developing recommendations for ONR management to coordinate with external S&amp;T investment. Examples include:·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Monitoring DARPA projects and supporting ONR participation in DARPA reviews.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Preparing S&amp;T roadmaps.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Monitoring Corporate OSD Prototyping and Concept Exploration programs (e.g. Joint Capability Technology·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Demonstration; Advancement of Science and Technology Priorities; Community of Interest Seedlings) to determine potential ONR benefit and courses of action.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting the DASN (RDT&amp;E) chartered Proposal Development Team.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting ONR interactions with the USD(R&amp;E) and Senior DoD Leadership.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Supporting ONR participation in the OUSD(R&amp;E) Deputies’ Action Group.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Provide operational and technical expertise, and administrative support to ONR sub-portfolio directors.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Manage the oversight of ONR funded Unmanned Aircraft operations.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Analyze external documents and recommend ONR courses of action and response.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Answer specific questions and inquiries about the ONR Programs and their relationships.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Bin, categorize, and analyze ONR 03 S&amp;T projects for trend analysis, portfolio understanding, and compiled aggregate results.·&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Prepare briefs and reports with results of analyses.

Senior Research Analyst

<h3>Job Description</h3>
Job Description
About Us:
Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.
*Please note: This is not a Talent Acquisition or HR-related role, the recruitment title is similar but unrelated. Job Summary:
Arizona Clinical Trials team is searching for qualified candidates to fill the Clinical Research Patient Recruitment Coordinator II position. This role is an integral part of the growing research team and serves as an educational resource for both patients and the patient recruitment team on clinical research eligibility and the benefits of new and innovative therapeutics.
Title: Research Recruitment Coordinator II Salary: $60,000 - $90,000 -- depending on experience, skills, and qualifications Status: Full-time, Exempt Location: Onsite in Peoria
Essential job functions/duties
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
<ul>
<li>Review standard of care (SOC) patients seen by providers who may qualify or be interested in participating in clinical trials.</li>
<li>Answer phone calls, social-media leads i.e. Facebook and/or other inquiries and use web-based systems such as Subject Well, Patient Navigator and/or sponsor provided portals to contact interested candidates. </li>
<li>Obtain HIPAA consent and enter subject data in electronic clinical trial management system</li>
</ul>
<ul>
<li>Evaluate participants through pre-screening and in-person interviews to ensure eligibility for the study.</li>
<li>Monitor, maintain, and find new study for screen fail subjects and those who have completed a study.</li>
<li>Contact potential subjects as per direction of providers.</li>
<li>Work alongside the Investigators, research nurses, research site managers, and clinical research coordinators to recruit new subjects into clinical trials and meet enrollment/exceed enrollment goals.</li>
<li>Assist research professionals with basic administrative and clinical procedures.</li>
<li>Provide all employees, research subjects, and interested candidates with an excellent service experience by consistently demonstrating professional decorum and knowledge of trials</li>
<li>Review and understand research protocols.</li>
<li>Contact past and potential participants who have expressed interest in clinical trials to determine eligibility through pre-screening </li>
<li>Provide study specific information not limited to study investigational product, potential side effects, duration of the study, compensation, etc.</li>
<li>Transfer pre-qualified candidates to research provider/investigator and delegated clinical research coordinator for final review and visit scheduling while ensuring transfer is successful.</li>
<li>Collaborate with community organizations and other external partners to facilitate recruitment.</li>
<li>Participate in weekend or after-hours recruiting events alongside providers and share results with patients.</li>
<li>Perform FibroScan and act as a general resource to patients and staff. </li>
<li>Participate in the training and orientation of new Research Recruitment Coordinators.</li>
<li>Maintain the company Research Board for actively enrolling studies. Actively review other informational documents and/or trial information portals.</li>
</ul>
<ul>
<li>Screen patient charts for actively enrolling studies.</li>
<li>Schedule appointments for eligible participants to attend the study.</li>
</ul>
<ul>
<li>Maintain accurate and complete participant records.</li>
<li>Attend research meetings and provide updates on recruitment activities.</li>
<li>Actively participate in the development of recruitment strategies.</li>
</ul>
Knowledge/Skills/Abilities Required
<ul>
<li>Experience and training in the conduct of clinical research and basic knowledge of medical terminology.</li>
<li>Bilingual English and Spanish -- written and spoken is highly preferred</li>
<li>Thorough understanding of the principles of GCP and biomedical research ethics.</li>
<li>Thorough understanding of clinical research trials and their enrollment status and goals.</li>
<li>Ability to work independently with minimal day-to-day supervision. </li>
<li>Ability to consistently recruit for moderate to advance complexity trials correctly and efficiently.</li>
<li>Strong attention to detail and commitment to ensuring patient confidentiality.</li>
<li>Must interact effectively with professional and administrative staff, sponsor, regulatory representatives, potential and current research subjects.</li>
<li>Strong organization, time-management, and leadership skills.</li>
<li>Advanced written and verbal communication skills.</li>
</ul>
Education, credentials, and/or trainings required:
<ul>
<li>Bachelor's Degree in healthcare, biosciences, or other related field required.</li>
<li>Master's Degree in healthcare, biosciences, or other related field preferred.</li>
<li>Good Clinical Practice (GCP) certification required.</li>
</ul>
Benefits &amp; Perks:
<ul>
<li>Health, Dental, Vision (with HSA plans and employer contribution)</li>
<li>3 weeks PTO</li>
<li>5 days Sick Time</li>
<li>7 Company holidays + 2 half-days</li>
<li>401K with company match (up to 6%)</li>
<li>Short &amp; Long Term Disability</li>
<li>Educational Assistance</li>
<li>Shared company vehicles for required travel</li>
</ul>
Travel requirements:
<ul>
<li>Some interoffice travel may be required with use of company vehicle or mileage reimbursement</li>
</ul>
Work authorization 
<ul>
<li>Must have valid documentation and authorization to work in the U.S. for any employer without sponsorship now or in the future. </li>
</ul>
EEO statement
It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate. 
[Notice to Staffing Agencies] It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly. We have an established and preferred network of contracted partners that we engage if and when we deem it necessary. We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly. Unsolicited resumes, onsite solicitations, and inquiries will not be considered or responded to. Overly persistent or forceful inquires may also be blocked across our network at the domain level as spam. Thank you for your understanding.

Research Patient Recruitment Coordinator II

<h3>Job Description</h3>
Job Description
About Dividend Assets Capital, LLC
Dividend Assets Capital, LLC is an employee-owned boutique wealth and investment management firm based in the heart of South Carolina's Lowcountry. With over a 40-year history of successful dividend growth investing at our foundation and a diverse, well-seasoned wealth and investment management team, we deliver personalized investment strategies and comprehensive wealth management services to our growing client base. We pride ourselves on bringing clarity, simplicity, and devotion to our clients, helping successful families, advisors, and institutions set and achieve their financial goals so they may preserve what is meaningful to them, their families, and their communities.
Position Summary
 
Dividend Assets Capital (DAC) is currently seeking a Senior Equity Analyst to join its growing investment team. This generalist equity research position will focus on identifying investments based on DAC's proprietary investment screens and performing fundamental research across several industries. Our disciplined investment process begins with bottom-up fundamentals and requires due diligence of industry and company-specific trends, company financial analysis, modeling, and valuation work. The Senior Analyst will then use this research to make specific investment recommendations for the client and institutional portfolios managed by DAC. The ideal candidate will be self-motivated with a high degree of personal and professional integrity. They also will value teamwork, be service-focused, and be able to work independently. This in-person opportunity (not remote or hybrid) is located in our Bluffton, SC office.
 
Responsibilities
 
• Learn and adopt DAC's dividend growth investment philosophy while embracing DAC's team-based culture, which supports an environment of mutual respect and shared rewards.
• Monitor DAC's existing equity investments, including posting quarterly earnings notes, maintaining price targets, and communicating current investment recommendations to Private Client and Institutional Asset Management teams.
• Screen DAC's investment universe to identify new opportunities within DAC's defined investment universe.
• Conduct a thorough fundamental analysis of a company's business and financial position, including cash flow assessment and dividend sustainability, balance sheet and income statement evaluation, and be able to draw insightful conclusions from their analysis.
• Responsible for all aspects of DAC's fundamental research process, including company research, setting up remote and in-person meetings with company management, writing company or industry research reports, developing detailed valuation analyses, and modeling financial projections.
• Monitor market conditions and evaluate current economic and investment trends.
• Communicate investment opportunities within DAC verbally and through written research reports.
• Contribute to DAC's client and institutional model portfolios as well as separate account non-model portfolios.
• Perform other duties as assigned by the Chief Investment Officer
• Be accountable and responsible for adhering to DAC's Core Values: Know Your Stuff, Devoted to Excellence, Serve With Integrity and Humility, Be Real and Transparent.
 
Qualifications
<ul>
<li>Bachelor's degree and completion or progress toward CFA® Level III are required; an advanced degree in Finance or Accounting is a plus</li>
<li>Minimum of 5 years of relevant experience (public or private equity investing)</li>
<li>Strong understanding of finance and accounting</li>
<li>Proficient with financial modeling and discounted cash flow analysis</li>
<li>Proficient in Word, Excel, and PowerPoint</li>
<li>Working knowledge of FactSet and/or Bloomberg</li>
<li>Strong communication skills, both written and verbal</li>
<li>Flexible and team-oriented, with the ability to pivot from one task to another with minimal supervision</li>
<li>Self-motivated and entrepreneurial, with a demonstrated passion for investing</li>
<li>Intellectual curiosity with an ability to engage in thoughtful debates over the merits of an investment.</li>
</ul>
 
If you're the right candidate and an offer is made, please note that we conduct a job-relevant, comprehensive background check and drug screen prior to your start date.

Sr. Equity Research Analyst

<h3>Job Description</h3>
Job DescriptionDescriptionAbout us We are Digital Science and we are advancing the research ecosystem.&nbsp;We are a pioneering technology company, and our vision is of a future where a trusted and collaborative research ecosystem drives progress for all. We believe in better, open, collaborative and inclusive research. In creating the next generation of tools and working in partnership with the community we tackle some of the biggest challenges to research. In order to achieve our vision, we need innovative, inspiring and dynamic people to join our team. Want to join us? Your new role Digital Science is seeking a highly analytical and engaging individual to serve as the on-site lead for the South Carolina Research Authority (SCRa) program. This hybrid role (3 days per week based out of Columbia, SC) blends deep analytical expertise with direct customer engagement to support institutions across the state utilizing Dimensions Research Security. You will deliver critical analytical insights, training, and community outreach to enable South Carolina research organizations to maximize data-driven, secure decision-making. What you’ll be doing This role is split between research analytics/data support (approx 60%) and training/engagement (approx 40%):
<ul>
<li>Liaison: Act as the primary on-site liaison between SCRa member institutions and Digital Science’s Academic Engagement and Product teams.</li>
<li>Data Delivery: Provide analytical and data support to SCRa and participating institutions, including reports, data extracts, and visualizations based on Dimensions Research Security.</li>
<li>Research Evaluation: Support research evaluation, landscape analysis, and benchmarking activities across portfolios, institutions, and research domains.</li>
<li>Methodology Development: Develop, test, and refine Boolean search strategies and methodologies for representing research topics and emerging fields.</li>
<li>Data Expertise: Maintain deep knowledge of Dimensions’ linked datasets (publications, grants, patents, policy, etc.) and their use in research security, strategy, and evaluation.</li>
<li>Collaboration: Collaborate with SCRa and Digital Science colleagues to identify key metrics, trends, and opportunities in the regional research ecosystem. </li>
</ul>
<ul>
<li>Lead Training: Lead training sessions, workshops, and onboarding programs for Dimensions users.</li>
<li>Feedback Loop: Capture and synthesize user feedback to inform product improvements and future engagement strategy.</li>
<li>Outreach: Promote awareness of new features, best practices, and responsible data use across the regional research community.</li>
<li>Engagement: Support the broader Digital Science Academic Engagement team in coordinating renewal, upsell, and satisfaction initiatives. </li>
</ul>
 What you’ll bring to the role
<ul>
<li>Analytical Background: 3+ years of experience in research analytics, evaluation, bibliometrics, science policy, or related fields.</li>
<li>Domain Knowledge: Strong understanding of the research and innovation ecosystem, including funders, research institutions, and government organizations.</li>
<li>Data &amp; Presentation: Proficiency in research data (publications, grants, patents) and familiarity with data visualization tools (e.g., Plotly, Tableau, matplotlib).</li>
<li>Training &amp; Communication: Proven experience designing and delivering interactive training and engagement sessions. Excellent written and verbal communication skills with demonstrated capacity for empathetic, customer-focused interaction.</li>
<li>Project Management: Ability to manage multiple projects and stakeholders across institutions in a collaborative environment.</li>
<li>Autonomy: Comfort working independently, with minimal supervision, in both on-site and remote settings.</li>
</ul>
<ul>
<li>Security Context: Experience supporting or analyzing national security-relevant research programs or sensitive data environments.</li>
<li>Compliance: Understanding of federal research compliance frameworks and research integrity principles.</li>
<li>Regional Expertise: Experience working with or within academic consortia or state-level research networks.</li>
<li>Platform Familiarity: Familiarity with Dimensions, Altmetric, or similar research intelligence platforms is highly desirable.</li>
</ul>
The following are highly desirable:
<ul>
<li>Familiarity with research intelligence platforms (e.g., Dimensions, Altmetric).</li>
<li>Experience with a coding or query language (e.g., Python, R, SQL).</li>
<li>Familiarity with data science environments and version control (e.g., Jupyter Notebooks, R Studio, VS Code, Git).</li>
</ul>
 Don't worry if you don't meet every qualification—let us be the judge! Studies show that many qualified candidates from under-represented groups hesitate to apply unless they meet every single requirement. We are dedicated to building a diverse and inclusive team and strongly encourage you to submit your application. Living our ValuesWe invest in, nurture and support innovative businesses and technologies that make all parts of the research process more open, efficient and effective.&nbsp; The talent we secure is fundamental to us achieving our vision and our growth plans. The values we live by are: We are brave in the pursuit of betterWe are collaborative and inclusiveWe are always open-mindedWe are from and for the community At Digital Science, our vision is to see research flow seamlessly – trusted, collaborative, and accessible – fueling breakthroughs that push humanity forward. This ambitious mission is one we achieve together, by enabling open, collaborative, inclusive research. We firmly believe that to truly innovate and solve the complex challenges faced by our customers, from researchers and universities to funders and publishers, we need diverse perspectives, experiences, and ideas. A rich mix of voices drives quality insights, fosters enhanced collaboration, and ultimately pushes knowledge forward more effectively. As an equal opportunity employer, we are committed to building and nurturing a workplace where every individual feels valued and belongs. All applicants will be considered for employment without attention to race, colour, religion, age, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Beyond recruitment, we strive to cultivate an environment where inclusivity is woven into the fabric of our culture, enabling everyone to be their best self and do their best work.

<h3>Job Description</h3>
Job Description
Cancer Partners of Nebraska (CPN) is seeking a Board-Certified Medical Physicist to join our growing Radiation Oncology department.
Lincoln offers a thriving university-town atmosphere with exciting sports, entertainment, restaurants and great quality of life. CPN is the largest cancer treatment center in Lincoln and it also provides oncology care for 12 critical access hospitals throughout Nebraska. We offer multiple cancer service lines under one roof, bringing together medical oncology, radiation oncology, gynecologic oncology, urologic oncology, genetic counseling, palliative care and clinical research. Our growing team includes 9 Medical Oncologists, 3 Radiation Oncologists, 1 Gynecologic Oncology Surgeon, 2 Urologists, 4 Medical Physicists, and 3 Dosimetrists.
General Summary of Duties
The physicist performs an important role working along with the radiation oncologist, the dosimetrist and others, to assure the accurate delivery of all aspects of a treatment prescription. Integrity and attention to detail are a must. This individual will work with the following software and equipment: Eclipse treatment planning, Aria R&amp;V system, MIM image management and contouring software, EZFluence, Clear Check, Varian Edge and TrueBeam accelerators, and GE CT Simulation with respiratory motion management.
Essential Duties and Responsibilities:
<ul>
<li>Demonstrates knowledge of human growth and development, assessment, range of treatment, and care of patients appropriate to the ages of the patients served.</li>
<li>Promotes customer service initiative.</li>
<li>Provides physics support to the Radiation Oncology Department.</li>
<li>Assists all cancer center employees in the technical aspect of Radiation Oncology.</li>
<li>Calibrates radiation therapy equipment in the radiation therapy department per departmental, state and/or federal requirements.</li>
<li>Implements and evaluates quality assurance programs for therapy equipment/department.</li>
<li>Verifies treatment plans.</li>
<li>Participates in chart rounds.</li>
<li>Participates in the Radiation Safety Program.</li>
<li>Monitors treatment planning software and implements new software updates.</li>
<li>Develops and implements physics aspects of all new treatment modalities.</li>
<li>Actively assists and supports departmental activities to assess and acquire appropriate equipment for treatment and quality assurance.</li>
<li>Participates in planning for future radiation oncology opportunities.</li>
<li>Understands the principles and concepts of Performance Improvement. Looks for opportunities and solutions for process improvements and seeks to improve job skills.</li>
<li>Maintains the principles of confidentiality. Understands the legal/regulatory requirements related to the release of information. Able to use the information systems pertinent to the job.</li>
<li>Oversees computerized treatment planning and associated tasks. Maintains ability to plan all treatment modalities.</li>
<li>Works with the IT department to install updates, and assures accuracy of data produced in treatment planning and quality assurance software.</li>
<li>Performs all duties associated with maintenance of state radiation licenses and assures that departmental functions meet state standards.</li>
<li>Actively participates in the QA program for radiation producing machines and associate equipment. Assists with correcting malfunctions of radiation producing machines or makes appropriate referrals to correct and/or repair units.</li>
</ul>
Education and Training:
<ul>
<li>PhDor M.S. in Therapeutic Radiological Physics</li>
<li>CAMPEP PhD or MS preferred</li>
<li>CAMPEP residency preferred</li>
</ul>
Experience:
<ul>
<li>Three years' experience preferred</li>
</ul>
Requirements:
<ul>
<li>Board Certification by the American Board of Radiology in Therapeutic Radiological Physics or equivalent required.</li>
</ul>

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