Our client ois looking for a Clinical Research Coordinator (CRC). He/she 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.
As a individual contributor you will be reporting to the appointed supervisor.
Qualities that our client are looking
➢ Independent learner, Meticulous and possesses good organizational and time management skills.
➢ Team player and work well with external collaborators and partners.
➢ Active participation in team / group activities or general interactions eg. meetings, discussions etc.
➢ Demonstrate willingness to learn and assume new roles & responsibilities/task assignments/projects (as applicable).
➢ Proactive in learning and helping other CRCs in issues with trial management
➢ Timely response/follow-up to email enquiries from sponsors/external parties.
➢ Able to provide clear, concise verbal &/or written communication.
Job Requirement:
➢ 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 Hematology / 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.
➢ Computer illiterate.
1 Year Contract ( september 2024 to august 2025)
22C1322
R23115755
