Associate Director, Clinical Pharmacology

The Associate Director of Clinical Pharmacology will provide support and strategic management for the design, and interpretation of clinical pharmacology studies, including first-in-human (FIH), dose-ranging, and healthy subjects and patient pharmacology trials. In this role, the Associate Director, Clinical Pharmacology will partner with Clinical Operations to ensure seamless integration of clinical pharmacology components into all clinical trials.

Lead, design and conduct of clinical pharmacology studies of increasing complexity, including leading the respective cross‑functional study team.

In collaboration with Clinical Development, Regulatory, and Biostatistics, design clinical pharmacology study protocols, study data analysis, modeling and simulation plans.

Participate in study protocol review discussions concerning scientific and procedural aspects of pharmacology study design.

Work with cross‑functional partners to address clinical issues arising from clinical pharmacology studies.

Maintain study timelines and resources to ensure timely and accurate execution of clinical pharmacology studies.

Anticipate problems that may arise in clinical trials and develop innovative solutions based on experience and creativity.

Adhere to regulatory requirements of study conduct and industry standards of Good Clinical Practice as well as internal SOPs.

Conduct PK‑PD and related analyses and provide clinical pharmacology input into data analysis / management plans and scientific review of literature.

Expertise in PK/PD modeling, dose selection, and regulatory strategy.

Analyze, interpret and author documents for clinical and regulatory submissions.

Present project updates and other key milestone information to cross‑functional partners and management.

Direct vendor collaborations for conducting clinical pharmacology studies.

Respond to questions from CROs and bioanalytical vendors to ensure quality operational conduct and compliance with GCP and quality standards.

Responsible for leading small cross‑functional project teams and managing clinical project deliverables through matrix management.

Responsible for contributing to development of clinical pharmacology related documents for Health Authority submissions.

Build and mentor a team of clinical pharmacology professionals and contractors.

Foster a culture of scientific excellence, collaboration, and continuous improvement.