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Vice President, Medical Affairs
Innovaderm Research Inc.. Develop and execute the long-term strategic vision for the Medical Affairs division with the CMSO .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in Medical Monitoring and Pharmacovigilance, with a strong focus on regulatory compliance, strategic oversight, and team leadership. Proven ability to manage P&L, drive collaboration across departments, and engage with sponsors in a commercial environment.
Highest-signal resume keywords
Medical Monitoring LeadershipPharmacovigilance OversightP&L ManagementRegulatory ComplianceClient Engagement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Medical MonitoringPharmacovigilanceRegulatory FrameworksBudget ManagementClinical Trial OversightSignal DetectionCase ProcessingQuality StandardsSOP DevelopmentAudit Defense
Soft Skills
LeadershipCollaborationMentoringCommunicationStrategic Thinking
Tools & Technologies
PV Safety DatabasesSafety Reporting Automation ToolsAI-Assisted Technologies
Certifications & Qualifications
Medical Doctor (MD, DO)Board Certification in Dermatology or RheumatologyAdvanced Business Training (MBA)
Industry Keywords
Pharmaceutical IndustryBiopharmaceutical IndustryClinical ResearchRegulatory InspectionsTherapeutic AreasHealth Authority InteractionsQuality Management System (QMS)Multilingual CapabilityInternational Regulatory Experience
About the role
Key responsibilities & impact- Develop and execute the long-term strategic vision for the Medical Affairs division with the CMSO
- Own the operating budget and P&L for Medical Monitoring and Pharmacovigilance
- Build capability roadmaps for Medical Monitoring and Pharmacovigilance
- Represent Medical Affairs on the Operational Leadership Team and advise the CMSO on medical, scientific, and safety risks
- Drive collaboration across Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Quality Assurance, Scientific Affairs, and Business Development
- Provide executive oversight of medical monitoring across Indero's clinical trial portfolio
- Lead physician resourcing, including hiring, training, deployment, and performance management
- Maintain medical monitoring SOPs, work instructions, and quality standards
- Escalate complex or high-risk medical monitoring issues and sponsor-facing medical disputes
- Provide strategic and operational oversight of pharmacovigilance, including case processing, signal detection, aggregate reporting, and regulatory submissions
- Ensure compliance with global and country-specific pharmacovigilance obligations
- Lead readiness for PV regulatory inspections and internal audits
- Partner with sponsors on PVAs and SDEAs
- Partner with Business Development on RFPs, client presentations, bid defenses, pricing, and new business
- Serve as senior medical point of contact for key sponsor accounts
- Represent Indero in scientific and industry forums
- Ensure Medical Affairs compliance with regulations, the QMS, and sponsor requirements
- Own Medical Affairs SOPs, quality plans, CAPA plans, and audit/inspection responses at executive level
- Lead, mentor, and develop the multidisciplinary Medical Affairs team
- Establish workforce planning, career pathing, succession planning, leadership development, performance frameworks, and KPIs
Requirements
What you’ll need- Medical doctor (MD, DO, or equivalent international medical degree) required
- 12-15 years of progressive experience in the pharmaceutical, biopharmaceutical, or clinical research industry
- 5-7 years in a leadership role within a CRO, pharmaceutical company, or hybrid organization
- Demonstrated experience leading and scaling Medical Monitoring and Pharmacovigilance functions
- Proven track record of client engagement in a commercial, revenue-generating environment
- Deep expertise in global clinical trial regulatory frameworks
- Meaningful exposure to multiple therapeutic areas
- Experience with health authority interactions, regulatory inspections, and audit defense
- Experience managing P&L or budget responsibility
- Board certification in dermatology or rheumatology is an asset but not required
- Advanced business training (e.g., MBA) is an asset but not required
- Working knowledge of PV safety databases and safety reporting automation tools
- Exposure to AI-assisted technologies in medical monitoring, PV, or medical writing workflows
- Published authorship of peer-reviewed scientific manuscripts or presentations at major clinical/scientific conferences
- Multilingual capability or international regulatory experience
- Ability to legally work in North America
- Willingness to travel frequently
Benefits
Comp & perks- Competitive compensation with performance incentives
- Full benefits
- Attractive advancement opportunities
- Stimulating work environment
- Remote role with frequent travel