Worldwide Clinical Trials
This role serves as a TMF Approver within the Records Management Compliance department, responsible for processing, reviewing, and resolving Trial Master File documents across both electronic and hard-copy formats. The position involves utilizing electronic document management systems to classify essential documents in strict adherence to Standard Operating Procedures and global clinical research regulations. Candidates are expected to report quality trends and provide administrative support to the RMC Lead while maintaining precise document control.
Headquarters
Durham, North Carolina, United States
Company Size
1001-5000 employees
Founded
1986
Worldwide Clinical Trials is a top-rated, full-service global CRO. We provide 30+ years of clinical expertise to benefit your study. Learn more about us here.
Worldwide Clinical Trials to acquire Catalyst
1 month ago
Worldwide Clinical Trials Completes Acquisition of Catalyst Clinical Research
3 weeks ago
Worldwide Clinical Trials to Acquire Catalyst Clinical Research, Expanding Oncology and FSP Capabilities
1 month ago
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Worldwide Clinical Trials.
Worldwide Clinical Trials didn’t post a salary, so this is our estimate from similar listings.
3% below the average for this role
Worldwide Clinical Trials appoints new CEO Alistair Macdonald
Sep 16, 2025
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