Roles & Responsibilities
Job Description
You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile relevant patients' data and maintain proper study documentation according to established protocols and regulatory requirements. Additionally, you will facilitate coordination of research studies with funding and regulatory bodies. Other duties include providing administrative support for Research Department when the need arises.
Requirements :
Interested applicants may apply at https : / / careers.singhealth.com.sg / job-invite / 1970 /
Tell employers what skills you have
Clinical Research
Healthcare
Administration
Data Entry
MS Office
Clinical Trials
Administrative Support
Nursing
Team Player
Regulatory Requirements
Life Sciences
Screening
Able To Work Independently
Research Coordinator • Islandwide, SG