Director, Clinical Pharmacology & Development Strategy

Haybury; Connecticut; On-site; USD 180,000 - 240,000; Full time

Job summary

Haybury, partners with a leading global biopharmaceutical company, seeks a Director-level Clinical Pharmacology Lead to own strategy across assets and development programs. You will integrate Clin Pharm, Pharmacometrics, and Non-clinical safety while guiding dose selection and modelling-based decisions.

You will mentor colleagues and influence milestones from early development through registration and launch, collaborating with Regulatory, Safety, Translational Medicine, and Commercial teams.

Qualifications

• PhD/PharmD/MD or equivalent advanced scientific qualification.
• Experience in Clinical Pharmacology beyond trial level.
• Strong PK/PD and regulatory submission experience.
• Familiarity with modelling & simulation including pharmacometrics.
• Experience in complex matrix organisations and stakeholder management.

Responsibilities

• Own and develop the Clinical Pharmacology strategy across multiple assets.
• Provide scientific leadership in PK/PD, DDI, formulation strategy and dose optimisation.
• Represent Clin Pharm, Pharmacometrics and Non-clinical safety on global project teams.
• Present scientific recommendations to project and governance teams.
• Lead Clinical Pharmacology input through milestones from early development to launch.
• Support regulatory strategy and global submissions.
• Collaborate with cross-functional partners in Clinical Development, Biostatistics, Regulatory Affairs, Safety, Translational Medicine, and Commercial.
• Mentor colleagues and advance Clinical Pharmacology capabilities.

Education

PhD, PharmD, MD or equivalent

Experience in Clinical Pharmacology beyond trial level

Tools

NONMEM

Job description

Haybury, partners with a leading global biopharmaceutical company, seeks a Director-level Clinical Pharmacology Lead to own strategy across assets and development programs. You will integrate Clin Pharm, Pharmacometrics, and Non-clinical safety while guiding dose selection and modelling-based decisions.

You will mentor colleagues and influence milestones from early development through registration and launch, collaborating with Regulatory, Safety, Translational Medicine, and Commercial teams.