Working Hours: 21hrs/ week
Location: Queenstown
Job Scope:
- Assist the investigators to recruit, screen, take consent and follow up participants of the study, in strict adherence to the study protocol and other applicable regulatory and ethical requirements.
- Coordinate collection and dispatch of biological specimens, and monitoring of adverse events and safety reporting.
- Handle entry and validation of study data, extraction of relevant information from medical records, reporting of adverse events, maintenance of investigators files and other essential documentation.
- Prepare and sort information before entering data into database and maintain data entry accuracy and quality levels to support team productivity and efficiency.
- Resolve incomplete information and data discrepancies.
- Coordinate scheduling and visits for stakeholders and study participants, as well as related finances (such as reimbursements) and logistics.
- Support in other functions such as general administration or coordination as required.
Job Requirements:
- Min. Bachelor's degree in health or life sciences, nursing or related field or equivalent
- Min. some working experience as CRC
- Prior work experience in clinical trials and/or project management in healthcare will be an advantage
For interested applicants, please send your updated resume to: [Confidential Information]
All candidates information will be treated with the strictest confidence
Melissa Zhang Zhiqi (Mezzo)
R2197564
Recruit Express Pte Ltd
99C4599
