Worldwide Clinical Trials
The Associate Director, Quality Management Systems provides enterprise leadership for regulatory intelligence, quality management document governance, and electronic Quality Management System processes. The role sets strategic direction, establishes governance and risk-based oversight, and drives organisation-wide implementation of evolving regulatory requirements across the GxP landscape. As a senior advisor to Quality Assurance leadership and cross-functional stakeholders, the role translates regulatory change into business priorities, sponsors complex transformation programmes, escalates material risks to senior forums, and ensures the organisation maintains compliant, inspection-ready, and sustainable quality systems.
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.
23% below the average for this role
Worldwide Clinical Trials appoints new CEO Alistair Macdonald
Sep 16, 2025
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