Specialist, Regulatory & Site Activation
Worldwide Clinical Trials
About this role
A Regulatory Affairs Specialist at Worldwide Clinical Trials manages regulatory submissions, coordinates with teams, and ensures compliance with international standards. The role involves maintaining documentation, reviewing materials, and supporting global clinical research projects.
Skills
Qualifications
About Worldwide Clinical Trials
worldwide.comWorldwide 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.
Recent company news
Clinical Trials ArenaWorldwide Clinical Trials to acquire Catalyst
1 month ago
Business WireWorldwide Clinical Trials Completes Acquisition of Catalyst Clinical Research
3 weeks ago
Applied Clinical Trials OnlineWorldwide Clinical Trials to Acquire Catalyst Clinical Research, Expanding Oncology and FSP Capabilities
1 month ago
European Pharmaceutical ReviewWorldwide Clinical Trials appoints new CEO Alistair Macdonald
Sep 16, 2025
Contract PharmaWorldwide Clinical Trials to Acquire Catalyst Clinical Research
1 month ago
About Worldwide Clinical Trials
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
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
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