Assistant Research Coordinator

Job Description

Job DescriptionBenefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Paid time off

Job description
We are looking for candidates in Huntsville, AL with a medical background and excellent interpersonal experience to support, facilitate, and organize daily human clinical trial activities. This person will be an integral part of the research team and play a part in the day-to-day running of human trials.

The following are a list of responsibilities:

experience with standard regulatory submissions (including 1572 and IRB)

review and execute trial activities as outlined in the study protocol

direct and participate in protocol training for research staff

obtain informed consent from potential subjects

write SOPs and update source documents as needed

organize subject binders

have a working knowledge of sponsor/FDA audits

GCP certified

previous clinical trial experience

computer skills are essential (incl. Excel, Adobe, Word, etc)

familiar with device skills including study devices, pt devices, iPhones, etc.

act as the liaison between regulatory authorities and the research team

other duties as needed

Personal Characteristics

honest, high integrity a must

highly organized, detail-oriented, meticulous and thorough

life learner

able to handle increased amounts of paperwork

compassionate and caring

able to work independently

self-motivator

**Salary based on experience. Benefits available if needed.