Global Pharmacovigilance Specialist
hace 3 días
Job Overview
Msd is a research-driven biopharmaceutical company dedicated to inventing medicines and vaccines for some of the world's most challenging diseases. We are seeking a highly skilled Senior Safety Data Specialist to join our team.
About the Role
- Process complex adverse event reports and ensure quality and compliance standards are met.
- Collaborate with Global Pharmacovigilance Case Management (GPVCM) management to identify process improvement opportunities and implement changes to increase efficiency and effectiveness.
- Assist with regulatory agency inspections and internal/external audits, preparing responses and implementing corrective actions as needed.
- Monitor and analyze key performance indicators to ensure adherence to processes and goals.
- Provide expertise on pharmacovigilance processes and procedures, conducting periodic assessments to ensure consistency and appropriateness.
Requirements and Qualifications
- Bachelor's degree in Health Care or related field; Master's degree desired.
- Advanced writing, reading, and speaking/listening English language skills.
- Minimum 2 years' experience in pharmacovigilance or related field.
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