Clinical Trial Coordinator
Institution:
National Skin Centre
Family Group:
Allied Health
Contract Type: 1 year contract
Roles & Responsibilities
- Develop enrolment/follow-up mechanisms, follow-up of study subjects
- Case report form (CRF) completion and study documentation
- Adverse event monitoring and reporting responsibilities
- Any other ad-hoc duties as assigned by Supervisor
Requirements
- Must have attained professional qualifications (Diploma) either in Nursing, health sciences or para-clinical disciplines
- Working knowledge of applicable regulations and guidelines e.g. SG-GCP, ICH-GCP, Code of Federal Regulations, Declaration of Helsinki, etc. will be advantageous
- Proficient in Microsoft Words, Excel
- Good written and spoken communication skills
- Able to work independently and as a team