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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>
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<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
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<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.

Chemical Engineer (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 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>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Applies the highest quality standard in all areas of responsibility</li>
<li>Demonstrates and promotes the company vision</li>
<li>Demonstrates strong client service skills, teamwork, and collaboration</li>
<li>Proactively plans and multitasks to maximize productivity</li>
<li>Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration</li>
<li>Regular attendance and punctuality</li>
<li>Applies 17025 compliance standards in all areas of responsibility, as appropriate</li>
<li>Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, GC-MS, ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.)</li>
<li>Operates and maintains job-related equipment as required</li>
<li>Performs advanced troubleshooting of laboratory equipment</li>
<li>Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipette verifications)</li>
<li>Performs laboratory tasks as assigned following supervisor direction, SOPs, WI, and other documentation</li>
<li>Assists other staff in the edits and updates of SOPs, WI, and other documentation</li>
<li>Follows all Good Documentation Practices appropriately, including digital platforms</li>
<li>Maintains working areas appropriately (cleaning, disinfecting, etc.)</li>
<li>Possesses strong organizational skills</li>
<li>Provides clear feedback</li>
<li>Keeps accurate records, follows instructions, and complies with company policies</li>
<li>Proactively checks and stays current with all training across multiple learning platforms</li>
<li>Provides instruction/training to new staff</li>
<li>Recognizes errors, identifies root causes, and applies process improvements</li>
<li>Provides analysis support for method validation as needed</li>
<li>Evaluates, reviews, and approves data by other analysts</li>
<li>Independently drafts, edits, and updates SOPs, WI, and other documentation</li>
<li>Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision</li>
<li>Makes recommendations for technical improvements, as needed</li>
<li>Assists in Method Development and executes method validation protocols</li>
<li>Assist in method transfer from the MDV group</li>
<li>Write validation protocols and reports</li>
<li>Communicates effectively with client staff members</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree in Chemistry, Biology, or other related degree concentration, or 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>7+ years of related experience</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 Winston-Salem, NC&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.

Senior Chemist GCMS Lab

<h3>Job Description</h3>
Job Description
A leading company in the cosmetics and chemical industry is seeking an experienced R&amp;D Research Scientist to join its team. This role involves product formulation, ingredient research, and regulatory compliance to support the development and enhancement of cosmetic and chemical products. If you have a strong background in product development and formulation, this is a great opportunity to advance your career. 
 Requirements
Key Responsibilities: 
· Develop and improve formulations for cosmetics and chemical-based products. 
· Conduct research on raw materials, active ingredients, and product stability. 
· Ensure compliance with cosmetic regulations and safety assessments. 
· Collaborate with internal teams to enhance product performance and innovation. 
· Optimize product textures, stability, and functionality through ingredient research and testing. 
 
Qualifications: 
· Degree in Chemistry, Chemical Engineering, or a related field. 
· Experience in cosmetics or chemical product development. 
· Strong understanding of formulation design and ingredient interactions. 
· Knowledge of cosmetic industry regulations and safety assessments. 
· Ability to conduct raw material analysis and apply innovative research to product development. 
 Benefits
Benefits: 
· Comprehensive Health Insurance 
· Paid Time Off (PTO) 
· 401(k) Retirement Plan 
· Performance-Based Employee Awards 
· Reimbursement for Business-Related Expenses 
· Complimentary Breakfast &amp; Lunch Provided 
 
If you are passionate about cosmetic and chemical innovation and eager to contribute to a cutting-edge R&amp;D team, apply today.

R&D Chemist - Cosmetics Products

<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>
Our company requires COVID-19 vaccinations for all current and future employees. Exemptions can be requested for those with a reasonable health or a religious/sincerely-held belief accommodation.
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
The European Institute of Policy Research and Human Rights is a prestigious institution that offers cutting-edge online programs designed to educate future leaders in policy research, human rights, and related disciplines. Our mission is to deliver world-class skill enhancing programs to candidates globally, equipping them with the knowledge and skills to influence policy and drive positive change in their communities.
Applications are invited for Senior Research Fellowship (for candidates enrolled / passed Masters / Doctoral in any discipline).
Program Overview
<ul>
<li>Learn and follow our methodology to draft research paper in one of the researchable areas. (No prior experience in research paper writing is required, Candidates will receive comprehensive mentorship and guidance throughout the process / tenure.) Program Certification fee of Eur498 is applicable. As a Certified Senior Research Fellow is a significant achievement a valuable addition to your CV that can impress future employers, universities, or scholarship committees. It helps set you apart with a unique edge.</li>
</ul>
What You'll Do:
<ul>
<li>Learn and Lead Groundbreaking Research: Know how to Tackle important policy issues and devise groundbreaking solutions.</li>
<li>Collaborate with Experts</li>
<li>Strategic Analysis: Utilize data to create influential policy recommendations.</li>
<li>Publish &amp; Impact: Contribute your findings to esteemed academic and policy publications.</li>
</ul>
Candidate will be choosing one of the researchable research areas for their research.
Research papers produced by candidates will be published with a Digital Object Identifier (DOI), ensuring the work is uniquely identifiable and accessible through our open-source publication portal.
Eligibility Criteria / Who Can Apply:
<ul>
<li>Open to candidates who are currently enrolled in or have completed a Masters or Doctoral program. Candidates enrolled or passed Bachelor degree but not enrolled in Masters are not eligible to apply.</li>
<li>Applicants from all academic disciplines are welcome, including but not limited to Law, Human Rights, International Relations, Management, Political Science, Social Sciences, Engineering, Medicine, Business, and related fields.</li>
<li>Working / non working professionals in any sector are encouraged to apply. This includes lecturers, professors, advocates, medical professionals, journalists, engineers, historians, managers, environmental scientists, government officials, social activists, and those involved in politics or any relevant field.</li>
<li>Candidates must demonstrate the ability to work independently in a virtual environment and effectively meet deadlines.</li>
</ul>
How to Apply
Interested candidates should submit their updated CV.
Shortlisted candidates will be contacted with complete details.

(SRFP)-Research Fellow-Senior (Code:EU4856)

Content Research Technician

Research & Analysis Roles

<h3>Job Description</h3>
Job Description
City of Bay City
Full Time - GIS Technician
Department of Public Works - U.W.U.A. Local 542
 
JOB SUMMARY
Observe and participate in GIS activities associated with data collection, georeferencing, digitization, asset management, and map creation. The focus will primarily be on GIS software, GPS technology, and data assurance. Gain experience working in a professional setting and develop an understanding of GIS technology and its applications in public service.
ILLUSTRATIVE JOB DUTIES AND RESPONSIBILITIES
An eligible applicant may be called upon to participate in any or all the following activities: (These examples do not include all tasks an applicant may participate in.)
<ul>
<li>GIS - Assist with the development, management, and maintenance of GIS data. This potentially consists of entering/updating attributes, digitization, data entry, georeferencing, basic cartography, the creation of meta data, and other duties as assigned.</li>
<li>GPS - Utilize GPS equipment to acquire coordinates on city assets as directed.</li>
<li>Create, develop, maintain scrips utilized for feature creation, data collection.</li>
<li>Create maps or other cartographic products for use by city staff.</li>
<li>Data collection and general research as directed.</li>
<li>Attend relevant staff meetings.</li>
</ul>
KNOWLEDGE, SKILLS AND ABILITIES:
The following generally describes the knowledge and ability required to enter the job and/or be learned within a short period of time to successfully perform the assigned duties.
<ul>
<li>Work requires physical presence at the job site to perform job duties.</li>
<li>Basic level of proficiency with ESRI software, ArcGIS Pro, Map, ArcGIS Online.</li>
<li>Basic knowledge of Java, xml, Python, or arcade scripting languages.</li>
<li>Basic knowledge of GIS principles.</li>
<li>Basic knowledge of cartographic principles.</li>
<li>Ability to interact with members of the public in a courteous and professional manner.</li>
<li>Ability to perform required job duties in a safe and responsible manner.</li>
<li>Good communication skills: ability to communicate effectively, both orally and in writing.</li>
<li>Ability to understand and carry out oral and written instructions.</li>
<li>Ability to work with minimal supervision and carry out assigned job tasks.</li>
<li>Ability to maintain positive working relationships with the public and other employees.</li>
<li>Ability to work effectively under time constraints and pressure.</li>
<li>High degree of mental, visual, and manual dexterity for sustained periods of time.</li>
<li>High degree of accuracy required.</li>
</ul>
ADDITIONAL QUALIFICATIONS
<ul>
<li>Must possess either a Certification in GIS or a four-year degree from an accredited degree program. or obtain either within 90 days of hiring. </li>
<li>Minimum GPA of 2.5 (3.0 preferred) (or diploma if recently graduated).</li>
<li>Must have a valid standard driver's license.</li>
<li>Must understand verbal and written materials and instructions; communicate effectively with the public, outside agencies, and city staff in a variety of situations.</li>
<li>Exhibit a level of proficiency using computers and general understanding of various software applications, such as Microsoft Suite products, and ESRI products.</li>
<li>Attendance and punctuality are essential functions of this position.</li>
<li>Must have an awareness of safety, understand the importance of safety, and be able to apply safety practices to the execution of all work.</li>
</ul>
Please see Full Job Description for more information
 Job Posted by ApplicantPro

GIS Technician

<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.
Job Description 
Eurofins is seeking a highly motivated and detail-oriented lab associate who will be responsible for qualifying and performing analytical methods to support particulate testing of drug products. This role will begin in&nbsp;January 2026. This individual will work directly on a client site in Boston, MA, supporting a multidisciplinary team of scientists and engineers. The candidate will contribute to a variety of CMC activities in a fast-paced, agile, and highly collaborative environment.
Key Responsibilities:
<ul>
<li>Routinely perform batch and stability testing of drug products using qualified methods.</li>
<li>Troubleshoot and resolve testing-related issues.</li>
<li>Maintain accurate records and documentation of test results.</li>
<li>Regularly perform analytical data review and reporting of results.</li>
<li>Participate in internal and external audits.</li>
<li>Stay current with the latest industry developments and regulatory requirements.</li>
<li>Aid in the development and qualification of particulate assays.</li>
<li>Support the technology transfer of analytical methods to external parties.</li>
<li>Maintain safe laboratory working conditions following GLP and EHS guidelines.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree with 0-2 years of industry experience, in Chemistry or a related field.</li>
<li>Hands-on experience with microscopy techniques such as: Flow Imaging Microscopy (FIM), Scanning Electron Microscopy (SEM), Fluorescent Microscopy preferred.</li>
<li>Experience with other methods for particle characterization (e.g. Raman) and counting (e.g. light obscuration) is also desirable.</li>
<li>General knowledge of cGMP, GLP, and regulatory requirements for biotech and pharmaceutical industries is highly desirable.</li>
<li>Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN) is a must.</li>
<li>Experience performing analytical data review and historical data evaluations.</li>
<li>Experience with writing SOPs and technical documents.</li>
<li>Familiarity with standard office software (MS Office, Teams, SharePoint).</li>
<li>Ability to work in a fast-paced, agile and highly collaborative environment is essential.</li>
</ul>
 Additional Information 
Position is full-time, Monday - Friday, 8:00 am - 5:00 pm.&nbsp; Candidates currently living within a commutable distance of Cambridge, MA, 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>
<li>Compensation is between 23.00-29.00 per hour, depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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