Senior / Clincial Research Coordinator (BILISG)(8997)

Roles & Responsibilities

The Clinical Research Coordinator will be responsible to, and work closely with, the Principal Investigator (PI), study team members and Family Medicine Development (FMD) team to ensure the successful timely completion of the research. The CRC’s principal role will be to work in general practices such as project management, recruitment, data collection, data entry and analysis. The CRC may be required to liaise with personnel from partnering institutions in the course of his / her work.

Responsibilities : Study Management

• Coordinate all aspects of research project from start-up to close-out
• Prepare and maintain regulatory documents
• Manage study timelines

Participant Recruitment and Management

Data Collection and Management

Regulatory Compliance

Administrative Duties

Requirements :

Tell employers what skills you have

Family Medicine

Regulatory Compliance

Clinical Research

Ability To Work Independently

Healthcare

Data Entry

Clinical Trials

Protocol

Audits

Nursing

Health Sciences

Life Sciences

Screening

IRB