At a Glance
- Tasks: Lead regulatory intelligence and QMS governance for transformative initiatives.
- Company: Worldwide Clinical Trials, a leader in clinical research.
- Benefits: Attractive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and excellence.
- Why this job: Drive impactful change in the GxP landscape and shape industry standards.
- Qualifications: Extensive experience in quality management systems and regulatory affairs.
The predicted salary is between 53438 - 65313 $ per year.
Worldwide Clinical Trials is seeking an Associate Director, Quality Management Systems to provide enterprise leadership for regulatory intelligence, QMS governance, and electronic QMS processes. The role sets strategic direction, governance, and risk oversight across the GxP landscape, translating regulatory change into business priorities and driving large-scale transformation initiatives.
As a senior advisor to Quality Assurance leadership, you will coordinate with cross-functional teams.
Senior Director, QMS & Regulatory Intelligence in Canberra employer: Worldwide Clinical Trials Holdings, Inc.
At Worldwide Clinical Trials, we pride ourselves on being an exceptional employer that champions innovation and purpose in clinical research. Our collaborative and inclusive work culture empowers employees to think creatively and take ownership of their roles, while offering ample opportunities for professional growth and development. Located in a vibrant environment, we provide a unique chance to contribute to life-changing therapies, ensuring that every team member's impact is valued and recognised.
Contact Details:
Worldwide Clinical Trials Holdings, Inc. Recruitment Team
