Senior Pharmacovigilance Specialist

reputed company Science is seeking a Senior Pharmacovigilance Specialist for a growing company located in Boston, MA. reputed company Pay: $50/hour Shift: Monday-Friday reputed company-5pm Employment Type: Full Time; 6 month contract with possible extension Work Model: Remote (Boston based preferred) Job responsibilities include: • Manage day-to-day case processing of adverse event records, ensuring accurate and reputed company documentation. • Support regulatory inspections and audits reputed company to pharmacovigilance activities. • Evaluate safety data and proactively identify potential safety signals. • Conduct medical evaluation of adverse event reports to assess severity and clinical relevance. • Prepare, analyze, and submit expedited and periodic adverse event reports to the FDA. • reputed company reconciliation of adverse event data with Medical Information, Product reputed company, and License Partners. • Ensure compliance with local and international regulations, guidelines, and applicable directives regarding adverse event handling. • Collaborate with internal teams, reputed company partners, and PV vendors to exchange and update safety information, including performing reconciliations. • Maintain thorough documentation to support regulatory requirements and audit readiness. • Contribute to reputed company process improvement initiatives reputed company the pharmacovigilance function. Qualifications: • Bachelor's degree in Nursing or a reputed company scientific field • Previous experience with safety systems including Argus and reputed company-G and clinical experience with AE/SAE assessments. • Previous Postmarketing Adverse Drug Experience is required along with experience working with service providers. Interested? Please apply today for immediate consideration! Apply tot his job Apply tot his job Apply To this Job