At a Glance
- Tasks: Manage GCP project implementations and ensure compliance across global teams.
- Company: Join Veeva Systems, a leader in clinical compliance and quality solutions.
- Benefits: Enjoy remote work flexibility, competitive salary, and professional growth opportunities.
- Other info: Dynamic role with opportunities to enhance your career in a fast-paced environment.
- Why this job: Make a real impact in clinical compliance while working with innovative global teams.
- Qualifications: Bachelor’s degree and 3+ years in Clinical QA with strong technical writing skills.
The predicted salary is between 45000 - 55000 £ per year.
Veeva Systems is seeking a Clinical Compliance Operations Specialist to manage GCP project implementations across multiple product lines, ensuring adherence to GCP, HIPAA, and CSV.
You will work with global teams to promote GCP compliance, author Gx P records, review deliverables, and support incident management.
The role requires a Bachelor’s degree, 3+ years in Clinical QA, strong technical writing, and knowledge of ISO 9001 and GCP.
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Remote: Clinical Compliance & GxP Quality Specialist employer: Veeva Systems
Veeva Systems is an exceptional employer, offering a dynamic work culture that prioritises employee success and innovation in the life sciences sector. With a commitment to professional growth through comprehensive development programmes and mentorship, employees are empowered to make a meaningful impact while enjoying the flexibility of a Work Anywhere policy. Located within commuting distance of London, Veeva provides a collaborative environment where new graduates can thrive and contribute to transformative solutions in healthcare.
