Clinical Research Coordinator (Marietta)

Position : Clinical Research Coordinator (RN)

Location : Marietta, GA

Duration : 6-month Contract to Hire

Schedule : Monday-Friday 8am-5pm

Hybrid - 4 days onsite, 1 day remote

Summary :

The Research Coordinator has general responsibility for managing clinical trials for the Clinical Trials Office at our client. This includes responsibility for identifying potential study patients; ascertaining patient eligibility for clinical trials; coordinating, evaluating, and following patients in clinical trials; coordinating therapy initiation and continuation; taking call for issues related to clinical trials; completing and filing necessary forms with internal and external departments and agencies as necessary; and maintaining records for patients enrolled in clinical trials.

Reponsibilities :

• Coordinates all facets of patient involvement in clinical trials.
• Conducts all aspects of clinical trial, including consenting, using Good Clinical Practice, FDA, and Institutional guidelines.
• Reviews patient chart for eligibility requirements and enrolls patient according to protocol guidelines.
• Communicates with physician / office staff regarding scheduling protocol specific requirements.
• Attends patient visits and gathers protocol-specific information when required.
• Communicates drug doses, protocol requirements and modifications to physician and office staff as appropriate.
• Coordinates dispersement of protocol provided drug therapy.
• Ensures that Investigation Product chain-of-custody practices are instituted and documented.
• Maintains accurate records for patients enrolled on clinical trials.
• Communicates effectively with Research Assistants and other research staff.
• Gathers appropriate source documentation
• Submits required documentation within designated time frame.
• Provides proper documentation of eligibility, treatment and follow-up requirements.
• Provides accurate research information to physicians and sponsors.
• Maintains a current chart on each protocol patient.
• Enters patient visits into clinical trial database.
• Ensures regulatory guidelines are followed.
• Ensures clinical trial and sponsor-required training is completed.

Requirements :