Cytel

Executive Consultant – Vice President, Quantitative Clinical Pharmacology

Cytel  •  United States (Onsite)  •  14 days ago
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Job Description

We are seeking an Executive Consultant – Vice President of Quantitative Clinical Pharmacology to join our Strategic Consulting team. This role blends scientific leadership, strategic advisory, client relationship development, and technical excellence in population modeling and quantitative clinical pharmacology. The successful candidate will leverage both deep quantitative expertise and strong business acumen to expand Cytel’s thought leadership, drive complex consulting engagements, and guide clients in shaping optimal regulatory and clinical development pathways.

Strategic Consulting & Thought Leadership

  • Serve as an externally recognized expert in Quantitative Clinical Pharmacology, Pop-PK/PK-PD modeling, MIDD, and quantitative regulatory strategies.
  • Lead the development and dissemination of innovative methodologies, contributing to Cytel’s scientific leadership through publications, conference presentations, and webinars.
  • Provide high-level strategic guidance to clients on clinical development plans, regulatory and market access pathways, trial design optimization, and quantitative decision-making.

Client Engagement & Business Development

  • Act as the primary point of contact for major Strategic Consulting accounts, ensuring delivery excellence and long-term partnership development.
  • Identify and pursue new business opportunities across Cytel’s consulting and analytics offerings, shaping solutions that meet revenue, profitability, and client satisfaction objectives.
  • Build and maintain relationships with senior stakeholders, including regulatory agencies (e.g., FDA, EMA), key opinion leaders, and executive-level client personnel.

Scientific & Analytical Leadership

  • Oversee and contribute to Pop-PK and PK/PD modeling, non-compartmental analysis (NCA), and broader QPP analytical activities.
  • Provide mentorship, technical oversight, and direction to consultants and analysts, building a high-performing quantitative team.
  • Support non-QPP engagements when needed, such as statistical design, adaptive/Bayesian methodologies, simulation-based planning, or data science initiatives.

Cross-Functional Collaboration

  • Work closely with Cytel’s business developers, statisticians, software teams, and data scientists to deliver integrated, high-value solutions.
  • Represent QPP expertise within multidisciplinary engagements, ensuring strategic alignment and scientific rigor.
  • Travel as required to engage with clients and internal stakeholders.

Experience

  • Minimum 5+ years of hands-on QPP experience; 15+ years overall experience in consulting, clinical development, or health research preferred for VP-level responsibilities.
  • Demonstrated leadership in MIDD, Pop-PK/PK-PD modeling, and quantitative strategy within drug development.
  • Experience interacting with regulatory authorities and contributing to regulatory submissions is highly desirable.

Required Technical & Professional Skills

  • Proven expertise in Pop-PK/PK-PD modeling, NCA, and interpretation of quantitative pharmacology results for CSR and reporting.
  • Proficiency in Phoenix WinNonlin/NLME, R, and strong understanding of computational and statistical methods used in clinical development.
  • Excellent technical writing, oral communication, and presentation skills; ability to clearly communicate complex quantitative concepts.
  • Strong organizational, analytical, and problem-solving abilities; able to operate effectively in a fast-paced, high-growth environment.

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Cytel

About Cytel

Cytel is the world’s leading data-science CRO, driving advancements in human health through robust analytics and innovative clinical trial software. For nearly four decades, we have set the standard in adaptive trial design, leveraging extensive data insights to inform strategy throughout every phase of drug development and commercialization. Our mission is clear: accelerate drug development, enhance success rates, and deliver better patient outcomes. With a comprehensive suite of services from innovative trial design to end-to-end biometrics and real-world evidence, our specialized, multidisciplinary team ensures optimal strategies for preclinical research, trial execution, market access, and reimbursement.

Headquartered in Cambridge, Massachusetts, Cytel has a global presence with over 2,000 employees across North America, Europe, and Asia. Learn more about how Cytel is harnessing the power of data to advance human health at www.cytel.com.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Cambridge, MA
Year Founded
1987
Website
cytel.com
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