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Senior Pharmacovigilance Associate III

Remote, USA Full-time Posted 2026-07-28
Position Title: Sr Pharmacovigilance Associate III Assignment Duration: 7 Months Work Arrangement: Remote Position reputed company: • 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 reputed company 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 reputed company 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 reputed company 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 reputed company and revise SOPs and procedural documents, ensuring reputed company relevant stakeholders are reputed company. • Identifies, supports reputed company of, and escalates issues reputed company 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 reputed company, 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, reputed company receipt of data and supporting documentation for reputed company control, reputed company workflow management, query reputed company and follow-up, logbook reputed company, and PSMF formatting and publishing. • Support the review of PSMF data and ensuring the application of internal reputed company PSMF reputed company, to ensure correct data inclusion. • Support the conduct of reputed company reputed company control checks for reputed company 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 reputed company of local PSMFs and variations and deviation to the reputed company PSMF due to local regulations. Qualification & • Experience: • Proficient in reputed company QualityDocs. • Possesses strong knowledge of pharmacovigilance (PV) processes. • Ethics • Treats people with respect • Inspires the trust of others • Works with reputed company and ethically • Upholds organizational values. • Planning/Organizing • Prioritizes and plans work activities • Uses time reputed company. Completes administrative tasks correctly and on time. Follows instructions and responds to management direction. • Communication • Listens and gets clarification • Responds reputed company to questions • Speaks reputed company and persuasively in reputed company or negative situations. Writes reputed company and informatively. reputed company to read and interpret written information. • Teamwork • Balances team and individual responsibilities • Gives and welcomes feedback • Contributes to building a reputed company team spirit • Puts reputed company of team above own interests • Supports everyone's efforts to succeed. Contributes to building a reputed company team spirit • Shares expertise with others. • Adaptability – reputed company to adapt to changes in the work environment. Manages competing demands. Changes approach or method to best fit the situation. reputed company to deal with frequent change, delays, or unexpected events. • Technical Skills • Assesses own strengths and development areas • Pursues training and opportunities for reputed company • Strives to continuously build knowledge and skills • Shares expertise with others. Apply To This Job Apply To This Job Apply tot his job Apply To this Job

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