Confidential
Senior / Clinical Research Coordinator
Not specifiedunknown
Skills
Bachelor’s degree in health sciences or nursingStrong interpersonal, communication (verbal and written), organizational and time management skillsAbility to work independently and as part of a teamProficient in MS Office applications (Word, Excel & Powerpoint)Meticulous and focused
About the role
Senior / Clinical Research Coordinator (BILISG) - Contract till July 2026 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 - Screen and recruit potential study participants - Obtain informed consent from participants Data Collection and Management - Collect, record, and manage study data accurately - Ensure data integrity and quality - Enter
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