The Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials Operations’ Standard Operating Procedures.
Key Responsibilities:
- Accomplish the study’s target enrolment as per agreed study timelines or shorter through effective recruitment strategies.
- Regular discussion or follow-up with study team on subject screening & recruitment rates eg. email communication or team meetings with Drs.
- Timely response/followup to email enquiries within 10 working days or less.
- Foster good working relationships and collaborate effectively across all streams to promote operational efficiency
- Invoicing is carried out on time and payment can be received with minimal delays.
Key Requirements:
- Degree in Nursing, Degree in Medicine, Pharmacy or Healthcare / biological sciences, preferably with experience in clinical trials or clinical research.
- 1-2 years experience in the conduct of clinical trials, specializing in Heamatology / Oncology interventional trials, governed under Health Product Act.
- Must have knowledge of setting up cell therapy trials.
- Must already been trained in ICH GCP.
- Meticulous and possesses good organizational and time management skills.
- Good communication and interpersonal skills.
- Independent learner, Meticulous and possesses good organizational and time management skills.
- Team player and work well with external collaborators and partners.
- Proactive in learning and helping other CRCs in issues with trial management
