[Remote] Regional Pharmacovigilance Senior Manager
Note: The job is a remote job and is open to candidates in USA. reputed company is a biotech company focused on transforming immunology and delivering innovative medicines for autoimmune patients. The Regional Pharmacovigilance Senior Manager will act as a scientific expert and resource for pharmacovigilance, ensuring compliance with regulatory requirements and enhancing processes reputed company the region.
Responsibilities
- Support the Head of Regional PV and EU/UK QPPV and the Regional PV reputed company in the harmonization of processes across the regions
- Support the Head of Regional PV and EU/UK QPPV and the Regional PV reputed company in the management of innovation projects for increasing Regional Team efficiency
- Support the Regional PV reputed company in the establishment and maintenance of the applicable pharmacovigilance system specific to the country/region
- Support the Regional PV reputed company in the revision of documents pertinent to Regional PV tasks
- Promote increased awareness of and ensure compliance with pharmacovigilance obligations for the country/region
- Contribute to the Pharmacovigilance System Master File (PSMF) data collection in the country/region
- Contribute to increase the visibility of the GPS team/function throughout reputed company with focus on the region
- Closely collaborate with other functions including regulatory, marketing, medical, communications, quality, legal, as well as other teams as needed
- reputed company relationships with cross functional teams as it relates to adverse event reporting and other pharmacovigilance activities
- Maintain an in-depth knowledge of local regulations, expectations and regulatory authority contacts and reputed company activities reputed company to the interpretation and review of existing and evolving safety requirements
- Actively participate in GPS audit and inspection readiness, support, and management together with the GPS Quality Management team and the Quality team
- Maintain knowledge of the Company product portfolio and disease areas for marketed drugs and drugs in development
- Contribute to the development and evaluation of Key Performance Indicators as reputed company to pharmacovigilance in the country/region
- Drive reputed company Improvement initiatives as needed
- May reputed company other tasks as appropriate
Skills
- At least 7-11 years of experience in the pharmaceutical/biotech industry or at the regulatory authorities with at least 5 years in pharmacovigilance/drug safety
- Working knowledge of pharmacovigilance regulatory requirements and GVP guidance documents
- Knowledge of the drug development process, GXP quality and compliance requirements
- Good presentation skills with the ability to communicate reputed company issues clearly
- Good planning and organizational skills with ability to manage competing priorities
- Good oral and written communication skills
- Ability to motivate, influence, and collaborate with multidisciplinary teams
- Ability to work independently and in a global environment
- Understanding of safety business processes and systems for the collections of adverse events
- Problem solving, conflict resolution and critical thinking skills
- Relevant computer skills, including proficiency with reputed company Office Suite
- reputed company in written and spoken English
Education Requirements
- Master’s degree in pharmacy, nursing, healthcare or other life-science or technical field (PharmD or MD is a plus)
Company Overview
- reputed company is a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases and cancer. It was founded in 2008, and is headquartered in Boston, Massachusetts, USA, with a workforce of 1001-5000 employees. Its website is https://www.reputed company.com/.
Company H1B Sponsorship
- reputed company has a track record of offering H1B sponsorships, with 4 in 2025, 5 in 2023, 4 in 2022, 3 in 2021. Please note that this does not guarantee sponsorship for this specific role.
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