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Clinical Research Coordinator
4 months ago
Busy independent Rheumatology Clinic is looking for a Full-time or Part-time will be considered to help run clinical drug trials and registries. We offer a four day work week, Monday through Thursday (10 hour days)
Must have GCP certification and prior experience as a clinical research coordinator or assistant.
Duties include:
Overseeing the trouble-free running of clinical trials.
Preparing and submitting IRB materials.
Managing budgets set aside for research.
Communicating with participants regarding study objectives and obtaining consent. Maintaining schedules of subject visits.
Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules.
Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards.
Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines.
Directing the collection, labeling, storage and transport of all specimens.
Making sure that all equipment and supplies needed for the study are in-stock and in good working order.
Job Types: Part-time, Full-time
Benefits:
- 401(k)
- Flexible schedule
- Health insurance
- Paid time off
Due to our patient population with auto-immune disorders, we do require staff to be up to date with Covid19 vaccinations.
