TMF Operations Specialist II - Precision & Compliance
Listed on 2026-10-02
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Quality Assurance - QA/QC
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Healthcare
Worldwide Clinical Trials in the United States is seeking a TMF Approver/QA Reviewer to ensure all Trial Master File documents meet regulatory requirements and company SOPs. You will process, review, and resolve TMF documents in electronic and hard copy formats, prepare quality control checklists, and participate in project team activities.
The role suits someone with up to 1–2 years TMF experience in CRO/Pharma, strong attention to detail, good written/verbal communication, and proficiency in
For the TMF Operations Specialist II
- Precision & Compliance position at Worldwide Clinical Trials, we are reviewing applications now.
We are currently recruiting a TMF Operations Specialist II
- Precision & Compliance for our team in United States.
This is an excellent position to take on the TMF Operations Specialist II
- Precision & Compliance role at Worldwide Clinical Trials.
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