Responsibilities:
- Provide research support service for clinical trials/research in accordance to ICH-GCP and protocol requirements
- Independently responsible for administration of clinical trials as assigned by Principal Investigator (PI) at his/her professional discretion
- Assist the sponsor or PI in the submission process for CIRB &/or HSA
- Handle complex commercial or IITs including overseeing recruitment of subjects
- Ensure full accountability of study equipment and investigational products during monitoring and study close-out
- Assist in quality control and prepare for quality assurance
- Provide instructions to Finance to issue invoices and handle communications between PI and sponsor companies
- Attend investigator meeting and start-up meeting for trials
Requirements:
- Degree in Life Sciences/Pharmaceutical Science and other related disciplines
- Fluent in written and spoken English and a 2nd language/dialect
- Intermediate computer skills (MS Office, Word and Excel)
- People-management skill, strong team-player
