Sr. Clinical Research Coordinator
The Sr. Clinical Research Coordinator (SCRC) ensures that clinical studies are conducted in accordance with the protocol, applicable regulations, Good Clinical Practice (GCP), and Institutional Review Board (IRB) requirements. This role goes beyond administrative duties to include subject recruitment, follow-up, data management, regulatory compliance, and training junior staff.
Responsibilities

+ Ensure study adherence to protocol and regulatory requirements.

+ Recruit, screen, and enroll study subjects while maintaining compliance.

+ Manage data entry and reporting, and keep detailed records.

+ Maintain communication with investigators, IRBs, sponsors, CROs, and regulatory authorities.

+ Assist with training and mentoring junior Clinical Trial Office staff.

+ Participate in investigator meetings, pre-study visits, and initiation meetings.

+ Collect and maintain accurate patient data ...