Vice President, Global Medical Affairs
What You'll Do:
Clinical Development & Medical Oversight
* Provide executive medical oversight across global clinical trials (Phases I-IV).
* Oversee medical monitoring activities including development and review of Medical Monitoring Plans.
* Ensure appropriate review and management of safety data, including Serious Adverse Events (SAEs), and other clinical parameters included in medical data review processes.
* Partner with Pharmacovigilance, Regulatory, and Quality Assurance teams to ensure compliance with global regulations.
* Serve as medical expert interacting with investigators, sponsors, and regulatory authorities.
* Support study design, protocol development, and feasibility assessments.
Business Development & Revenue Generation
* Lead and contribute to RFP responses, including strategy, content, and medical positioning.
* Participate in bid defense meetings, client presentations, and capabilities discussions.
* Partner with Commercial/Sales teams to identify growth opportunities and expand client relationships.
* Provide strategic medical input to win new business and increase revenue.
* Represent the organization at industry events, conferences, and client meetings.
Consulting & Scientific Leadership
* Provide medical leadership for consulting engagements and drug development programs.
* Oversee development of clinical documents including protocols, CSRs, regulatory submissions, and publications.
* Serve as subject matter expert for advisory boards and client engagements.
* Ensure scientific integrity across all deliverables.
Operational & Strategic Management
* Develop and execute Medical Affairs strategy aligned with company growth objectives.
* Oversee departmental budgeting, forecasting, and resource allocation.
* Ensure development and maintenance of SOPs and implementation of best practices, creating an environment of continuous improvement.
* Drive process improvements to enhance quality, efficiency, and client satisfaction.
* Oversee administrative policies and processes associated with managing the Medical Affairs function, ensuring team members meet foundational expectations of their role.
People Leadership & Talent Development
* Attract, develop and retain team members.
* Coach and mentor Medical Directors, and Medical Affairs staff, and others as needed.
* Drive performance management, succession planning, and team capability building.
* Provide training and ongoing education for internal teams.
What You'll Bring:
* 10 years of progressive experience in the CRO, pharmaceutical or biotech industry.
* Significant clinical research experience including medical monitoring.
* Deep scientific, regulatory, clinical trial or drug development experience.
* Thorough knowledge of relevant FDA and other international health authorities' regulations and guidelines, including directly intera...
- Rate: Not Specified
- Location: Covington, US-KY
- Type: Permanent
- Industry: Finance
- Recruiter: CTI Clinical Trial Services, Inc.
- Contact: Not Specified
- Email: to view click here
- Reference: VPGLO001860
- Posted: 2026-08-06 08:42:24 -
- View all Jobs from CTI Clinical Trial Services, Inc.
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