Vice President / Executive Director, Clinical Pharmacology - High-growth Biotech
发布于: 22/07/2026
shanghai East China
Permanent
生命科学、医疗保健、制药
About the Company
- Our client is an innovation-driven biotechnology company focused on advancing differentiated therapies in neuroscience, pain management, and other areas of significant unmet medical need.
- The organization is building a world-class R&D platform and seeks an experienced Clinical Pharmacology leader to drive data-driven development strategies from First-in-Human (FIH) studies through late-stage clinical development and global regulatory submissions.
About the Job
This is a strategic leadership role responsible for defining and executing clinical pharmacology strategies across the company’s pipeline. The successful candidate will serve as a key scientific leader, leveraging modeling and simulation approaches to optimize clinical development decisions, accelerate proof-of-concept validation, and support global regulatory interactions.
- Develop and lead integrated clinical pharmacology strategies across multiple development programs, ensuring alignment with overall clinical and regulatory objectives.
- Design and oversee Phase I–III clinical pharmacology programs, including First-in-Human studies, dose-escalation strategies, dose selection, exposure-response assessments, and dosing regimen optimization.
- Lead the design, execution, interpretation, and reporting of PK/PD studies to support clinical development and registration strategies.
- Establish quantitative pharmacology frameworks to characterize exposure-response relationships, inform benefit-risk assessments, and support proof-of-concept (PoC) decision-making.
- Apply advanced Modeling & Simulation (M&S) methodologies, including PBPK, PopPK, PK/PD, and exposure-response modeling, to optimize development plans and reduce clinical development risk.
- Lead clinical pharmacology contributions to regulatory submissions, including IND, NDA, and global registration packages.
- Support regulatory interactions with agencies such as the FDA and NMPA by preparing clinical pharmacology briefing materials, responses to regulatory questions, and participating in formal agency meetings.
- Develop and implement innovative biomarker strategies, particularly in neuroscience, CNS, and pain-related indications, to support translational medicine and early clinical decision-making.
- Provide scientific leadership in the interpretation of pharmacokinetic, pharmacodynamic, efficacy, and safety data throughout the product lifecycle.
- Collaborate closely with Clinical Development, Medical Affairs, Clinical Operations, Biostatistics, Regulatory Affairs, Translational Medicine, and Nonclinical Research teams to ensure integrated development strategies.
- Influence portfolio decisions by providing quantitative insights regarding dose selection, trial design, probability of success, and development risk.
- Build and lead a high-performing Clinical Pharmacology organization, including recruitment, mentoring, capability development, and succession planning.
- Establish and expand internal Modeling & Simulation platforms and best practices to enhance organizational scientific capabilities.
- Serve as a recognized technical expert and strategic advisor to executive leadership on clinical pharmacology and quantitative drug development.
Required Qualifications
- PhD in Clinical Pharmacology, Pharmacokinetics, Pharmaceutical Sciences, Pharmacometrics, or a related scientific discipline.
- Minimum 8 years of experience in Clinical Pharmacology, Pharmacometrics, PK/PD, or Quantitative Clinical Pharmacology within the biotechnology, pharmaceutical, or CRO industry.
- At least 3 years of leadership experience managing clinical pharmacology, pharmacometrics, or quantitative sciences teams.
- Prior experience as a Clinical Pharmacology Lead or Head of Clinical Pharmacology within an innovative drug development environment is highly desirable.
- Demonstrated experience leading clinical pharmacology strategies for at least two innovative drug programs from First-in-Human studies through Phase III clinical development.
- Proven success supporting IND and/or NDA submissions with FDA, NMPA, or other major regulatory agencies.
- Experience in neuroscience, CNS, pain management, or related therapeutic areas is strongly preferred.
- Deep expertise in PK/PD modeling, exposure-response analysis, and quantitative drug development methodologies.
- Advanced proficiency with industry-standard modeling tools such as NONMEM, Monolix, R, Phoenix NLME, Simcyp, GastroPlus, or equivalent platforms.
- Hands-on experience with PBPK, PopPK, PK/PD modeling, exposure-response analysis, model-informed drug development (MIDD), and simulation-based decision-making.
- Comprehensive understanding of contemporary drug development processes, translational medicine strategies, and regulatory expectations related to clinical pharmacology.
- Strong scientific publication, technical writing, and regulatory documentation skills.
- Excellent analytical thinking, problem-solving, and data interpretation capabilities.
- Proven ability to influence cross-functional teams and communicate complex scientific concepts to senior stakeholders and regulatory agencies.
- Fluent English communication skills, with the ability to independently prepare and review clinical protocols, reports, study documents, and regulatory submissions.
Why This Opportunity?
- Lead the clinical pharmacology strategy for a growing pipeline of innovative therapies and directly influence key development decisions from FIH through registration.
- Build and shape a Clinical Pharmacology and Modeling & Simulation function, creating long-term scientific capabilities within a high-growth biotech environment.
- Work at the forefront of quantitative drug development, applying advanced MIDD, PK/PD modeling, and biomarker strategies to accelerate innovation.
- Partner closely with executive leadership, regulatory authorities, and leading scientific experts to drive global development programs.
- Make a meaningful impact on the development of novel therapies addressing significant unmet needs in neuroscience, pain, and other serious diseases.