Assistant Research Coordinator

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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.

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

• 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

• 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.

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