Senior Pharmacovigilance Associate III

Position Title: Sr Pharmacovigilance Associate III

Assignment Duration: 7 Months

Work Arrangement: Remote

Position Summary:
• Support GPS procedural document management activities including the creation, review, and revisions of controlled documents, policies and procedures.
• Support the maintenance of the Global PSMF, local PSMFs and annexes on a regular basis to ensure that content accurately reflects our organization PV processes and compliance with regulatory requirements in an expedited manner.

Background &
• Context:
• The role focuses on Global Patient Safety (GPS) standards and the maintenance of Pharmacovigilance System Master Files (PSMF) to ensure global regulatory compliance.

Key Responsibilities:
• Ensures high service level to GPS stakeholders by advising on document strategy for GPS teams and supports content development for specific procedures across multidisciplined teams.
• Leads the development of procedural documents across multidisciplinary teams, ensuring appropriate input from cross-functional GPS groups and relevant business functions.
• Supports the end-to-end Document Change Control process.
• Collaborates closely with GPS management, subject matter experts, and other functions to develop and revise SOPs and procedural documents, ensuring all relevant stakeholders are engaged.
• Identifies, supports resolution of, and escalates issues related to procedural documents as needed.
• Demonstrates strong document writing skills, with the ability to create, update, and refine process steps, descriptions, and responsibilities in line with document standards.
• Drives global harmonization of procedural documents to ensure clarity, consistency, and alignment with our organization documentation hierarchy and conventions.
• Support the end-to-end management of Global and/or Local PSMFs, including data collection, timely receipt of data and supporting documentation for quality control, Veeva workflow management, query resolution and follow-up, logbook generation, and PSMF formatting and publishing.
• Support the review of PSMF data and ensuring the application of internal core PSMF strategy, to ensure correct data inclusion.
• Support the conduct of timely quality control checks for each PSMF contribution, including but not limited to PSMF Narrow Reviews and PSMF Consistency Checks for Global and Local PSMF.
• Participating and supporting in Audits and Inspections as a PSMF SME.
• Maintains oversight of local PSMFs and variations and deviation to the Core PSMF due to local regulations.

Qualification &
• Experience:
• Proficient in Veeva QualityDocs.
• Possesses strong knowledge of pharmacovigilance (PV) processes.
• Ethics
• Treats people with respect
• Inspires the trust of others
• Works with integrity and ethically
• Upholds organizational values.
• Planning/Organizing
• Prioritizes and plans work activities
• Uses time efficiently. Completes administrative tasks correctly and on time. Follows instructions and responds to management direction.
• Communication
• Listens and gets clarification
• Responds well to questions
• Speaks clearly and persuasively in positive or negative situations. Writes clearly and informatively. Able to read and interpret written information.
• Teamwork
• Balances team and individual responsibilities
• Gives and welcomes feedback
• Contributes to building a positive team spirit
• Puts success of team above own interests
• Supports everyone's efforts to succeed. Contributes to building a positive team spirit
• Shares expertise with others.
• Adaptability

– Able to adapt to changes in the work environment. Manages competing demands. Changes approach or method to best fit the situation. Able to deal with frequent change, delays, or unexpected events.
• Technical Skills
• Assesses own strengths and development areas
• Pursues training and opportunities for growth
• Strives to continuously build knowledge and skills
• Shares expertise with others.