Pharmacovigilance Sciences Manager (Remote)
Job Description
General Summary: The Patient Safety Pharmacovigilance (PV) Sciences Manager will be responsible for the preparation of aggregate safety reports, including PSURs, PADERs, and DSURs, for assigned Vertex products, marketed or in development. The PV Sciences Manager will collaborate closely with Patient Safety Physicians on product safety teams and in supporting risk management activities, including signal detection and tracking, Regulatory Authority requests, and maintenance of risk management plans (RMPs). Key Duties And Responsibilities- Contributes to PV Sciences activities for Vertex products, marketed or in any phase of development
- Prepares aggregate safety reports, including establishment of timelines, content and project management, safety database report requests, review of data, and compilation of information
- Supports Disease-area Safety Team (DAST) through meeting preparation and conduct, signal detection/tracking, RMP development and maintenance, and other risk management activities
- Conducts literature search results in collaboration with the Patient Safety Physician for identification of potential safety issues/signals and inclusion in aggregate safety reports
- Collaborates with Regulatory Affairs and other functions to coordinate submission of aggregate safety reports
- Collaborates with Quality, Standards & Training to ensure aggregate safety report procedures, training, and activities are sufficiently defined and maintained.
- Participates in departmental development activities including SOP and Work Instruction development, Audits and Inspections.
- Performs other duties as assigned
- Demonstrates strong ability to communicate effectively to exchange complex information with others
- Exhibits ability to multi-task effectively
- Demonstrates solid written and oral communication skills, and sound attention to detail
- Ability to analyze, interpret, and summarize moderately complex data with general oversight
- Exhibits firm comprehension of established procedures
- Applies good understanding of industry practices for drug development and PV
- Demonstrates basic knowledge of related disciplines, and an understanding of general concepts and experiential detail within those areas
- Possesses computer skills to support use of electronic systems and development of writing deliverables
- PharmD, PhD, MPH, advanced healthcare degree, or equivalent professional experience
- Typically requires 3 years of experience in pharmacovigilance or relevant experience with, data analysis and medical/scientific writing
- Remote: work remotely five days per week and come into the office on occasion – you’re always welcome on-site; or select
- Hybrid: work remotely up to two days per week; or select
- On-Site: work five days per week on-site with ad hoc flexibility.
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