Clinical Executive Consultant - Vice President
- Serve as an externally recognized thought leader in clinical development, regulatory strategy, market access strategy, and quantitative clinical methods.
- Provide strategic guidance to clients on optimizing clinical development plans, trial design, decision-making frameworks, and evidence generation.
- Develop new methodologies and thought leadership materials for dissemination through conferences, publications, and webinars.
- Lead business development, account management, and project execution across a broad and growing client portfolio.
- Identify emerging client needs and shape innovative solutions aligned with Cytel’s revenue, quality, and customer satisfaction objectives.
- Act as the primary point of contact for Strategic Design Consulting engagements, developing trusted, long-term partnerships with clients.
- Apply deep clinical development knowledge to design, initiate, and conduct effective clinical studies, integrating novel principles where appropriate.
- Serve as a subject matter expert for assigned accounts and therapeutic areas, collaborating with consultants and associates across Cytel.
- Maintain strong engagement with senior client leadership, regulatory agencies (FDA/EMA), and key opinion leaders to support and refine development strategies.
- Mentor and motivate a high-performing team of consultants and analysts; model excellence in strategic thinking and scientific rigor.
- Represent Cytel across the industry, demonstrating strong interpersonal leadership and the ability to influence stakeholders at all levels.
- Participate in cross-functional collaboration within Cytel’s Strategic Consulting and other business units.
- MD, MD/PhD; subspecialty training and/or clinical practice experience desirable.
- 10+ years of experience in consulting, clinical trials, or health research environments.
- Demonstrated ability to understand and influence customer decision-making processes, with a track record of identifying and capturing transformational opportunities.
- Deep understanding of the biopharmaceutical R&D process, complemented by strong business acumen and appreciation of broader organizational and industry dynamics.
- Proven strategic thinker with global orientation, strong analytical skills, and the ability to execute tactically in complex environments.
- Demonstrated success in leading teams, mentoring junior colleagues, and driving high-impact consulting engagements.
- Experience interacting with regulatory agencies (FDA/EMA) and key opinion leaders to shape and enhance development plans.
- Ability to design and execute modern clinical studies and integrate them into cohesive clinical development strategies.
- Strong knowledge of disease areas or technical domains relevant to product development.
- Thorough understanding of clinical regulatory requirements, ICH/GCP guidelines, and ethical standards.
- Collaborative, entrepreneurial, self-motivated, and comfortable working in fast-paced, high-growth environments.
- Play an integral role in shaping the future of drug development for clients worldwide.
- Contribute to an exciting new chapter in Cytel’s history, with opportunities for growth and advancement into senior leadership roles.
- Work alongside and learn from some of the most innovative and influential minds in the industry.
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