FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Senior Director – Executive Director, Medical Writing
ERGOMEDSenior Director leading the Medical Writing function for global pharmacovigilance operations. Overseeing a high-performing team and ensuring compliance with global regulations and standards.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in pharmacovigilance and PV Medical Writing, with a strong focus on regulatory compliance and quality assurance. Proven leadership in managing high-performing teams and driving continuous improvement initiatives in medical writing.
Highest-signal resume keywords
Pharmacovigilance ExperiencePV Medical Writing ExpertiseLeadership and People ManagementRegulatory Compliance SupportAggregate Safety Report Authoring
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
PV Medical WritingAggregate Safety Report AuthoringPV Procedure DevelopmentRegulatory ComplianceQuality AssuranceInspection ReadinessContinuous Improvement Initiatives
Soft Skills
Team LeadershipStrategic ThinkingCollaboration
Industry Keywords
Global Pharmacovigilance RegulationsPharmacovigilance
About the role
Key responsibilities & impact- Lead the PV Medical Writing function
- Manage and develop the PV Medical Writing team
- Drive quality, compliance, inspection readiness, and continuous improvement initiatives
- Provide strategic PV medical writing expertise and subject matter leadership
- Support business development activities
Requirements
What you’ll need- 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
Benefits
Comp & perks- Work in a global pharmacovigilance specialist environment
- Opportunities for professional growth and development
- Collaborative team culture
- Flexibility in work arrangements