Clinical Trial Assistant

15 hours ago

Singapore PRESTIGE BIOPHARMA LIMITED Full time

**Job Overview:
**Key Responsibilities**:

- Serve as the unblinded point of contact for logistics vendors and unblinded CRAs.
- Generate and review shipment documents, including batch records, Certificate of Conformance (CoRC), temperature logger data, etc.
- Manage investigational product (IP) inventory and ensure proper storage and distribution.
- File unblinded Trial Master File (TMF) documents in accordance with regulatory requirements.
- Review unblinded monitoring reports and address any discrepancies or issues as needed.

**Qualifications**:

- Good emotional intelligence skills, with the ability to communicate effectively and maintain professionalism in challenging situations.
- Ability to work independently and manage multiple tasks simultaneously, with strong attention to detail.
- At least 1 year of experience in relevant experience managing clinical trials in a pharmaceutical company, CRO, or clinical trial site.
- Bachelor's degree in a relevant field (e.g., life sciences, healthcare, etc.) preferred.

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