PV Compliance Specialist
7 days ago
Job Summary
We are seeking a highly skilled PV Compliance Specialist to join our team at Bristol Myers Squibb. As a PV Compliance Specialist, you will be responsible for ensuring the safety of our medicines by monitoring safety outputs and ensuring compliance with global regulatory requirements.
Key Responsibilities
- Provide compliance oversight through ongoing monitoring of safety outputs created by WWPS to ensure continuous compliance and quality excellence with all applicable safety guidelines and regulations.
- Ensure ongoing regulatory compliance and mitigation of potential risks associated with PV activities delivered by WWPS.
- Contribute to the development of efficient and effective compliance monitoring programs and processes as well as the PV compliance tools and dashboards that support compliance programs.
Requirements
- A minimum of 5 years pharmaceutical industry experience, including 3 years of pharmacovigilance, drug development, clinical development or regulatory affairs experience specifically involving Safety Database case processing.
- Prior experience in IT project management including the skills for JIRA management, HP ALM, and share point management is preferred.
- Strong scientific background in a life science related field.
- Prior quality related experience in pharmacovigilance preferred.
What We Offer
Bristol Myers Squibb is a diverse and inclusive company that offers a range of benefits and opportunities for growth and development. We are committed to creating a work environment that is safe, inclusive, and respectful of all employees.
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