Clinical Trial Coordinator

1. Coordinate clinical trial start-up, daily activities and close-out.
2. Assist with patient screening, informed consent, study assessments and timely adverse event reporting.
3. Ensure trials follow study protocols, GCP guidelines and regulatory requirements.
4. Track trial expenses, assist with invoicing and support research account closure.
5. Maintain accurate trial data, documents and specimen records, and assist with monitoring visits and audits.

By submitting your application or résumé to PickPros Pte. Ltd., you consent to the disclosure of your personal information to prospective employers for recruitment purposes. Only shortlisted candidates will be notified. All applications will be treated confidentially.

PickPros Pte. Ltd. | EA Licence No.: 26C3710