Director, R&D Scientific Engagement Strategy & Operations
$216,000–$264,000 year
On-siteConshohocken, Pennsylvania, United States
Job Summary
Lead R&D external scientific engagement strategy by managing consultant relationships, advisory boards, and steering committees, including scope definition, contracting, and payment oversight. Own end-to-end execution of R&D participation at scientific congresses and professional society meetings, defining objectives, coordinating attendance, and implementing structured debrief processes to capture actionable insights. Partner cross-functionally with Legal, Compliance, Finance, Medical Affairs, and Commercial stakeholders to ensure all activities align with strategic priorities and maintain strict regulatory adherence. Maintain audit-ready documentation for all external interactions and financial transactions while driving measurable strategic value from scientific engagements. Support broader R&D operational initiatives, including annual planning, budgeting, and resource allocation, ensuring coordinated execution across the organization.
Required Qualifications
- Bachelor's degree in scientific or relevant business discipline
- 12+ years of experience in pharmaceutical/biotechnology industry operations, clinical development, or related functional area
- Proven experience managing complex operational processes, external engagements, and cross-functional initiatives in a matrixed environment
- Demonstrated ability to influence senior leaders and drive alignment across R&D, compliance, medical affairs, and commercial partners
- Strong business acumen, organizational skills, and ability to translate strategy into operational execution
- Excellent communication and presentation skills, with experience preparing executive-level summaries and operational reporting
- Proficiency in data analysis, metrics development, and reporting tools
- Advanced skills in PowerPoint, Excel and business intelligence tools
Desired Qualifications
- Applicable advanced degree (e.g., MS, MBA, PhD, MD)
- Experience with scientific meeting strategy and congress planning
- Familiarity with clinical development processes, drug development lifecycle, regulatory environment, and R&D organizational structures
- Prior exposure to consultant advisory boards, expert engagements, or steering committee oversight
- Experience in project management or management consulting
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