Senior Director / Executive Director Medical Writing
HybridBelgrade, Central Serbia, Serbia
Job Summary
Lead the PV Medical Writing function, ensuring high-quality, compliant, and timely deliverables while managing and developing the team to foster performance and growth. Drive quality, compliance, and inspection readiness initiatives, including oversight of SOPs, KPIs, audits, and regulatory inspections. Provide strategic PV medical writing expertise to clients and internal stakeholders, support business development activities like proposals and bid defenses, and oversee departmental resources and budgets. Review regulatory safety responses, contribute to Risk Management Plans, and aggregate reports. Build strong client relationships and represent the organization externally through industry engagement and publications.
Required Qualifications
- Extensive pharmacovigilance and PV Medical Writing experience
- Leadership and people management of high-performing teams
- Deep knowledge of global pharmacovigilance regulations
- Expertise in authoring and reviewing aggregate safety reports and PV procedures
- Proven experience supporting regulatory compliance, inspections, and pharmacovigilance system oversight
- QPPV or Deputy QPPV responsibilities
- Strong business acumen
- Experience supporting proposals, client engagements, and bid defense activities
- Excellent scientific, regulatory, and analytical capabilities
- Translating complex clinical and safety data into clear, high-quality regulatory and scientific documents
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