Senior Director, Clinical Pharmacology

Description of Role Centessa is seeking an experienced Senior Director, Clinical Pharmacology to provide scientific and strategic leadership for clinical pharmacology across a diverse pipeline spanning early development through late‑stage and registrational programs. Reporting to the Executive Director, Clinical Pharmacology, this position is accountable for developing and executing clinical pharmacology strategies that address the unique challenges of neuroscience drug development, including CNS exposure, dose optimization, and translational relevance. The Senior Director partners closely with cross‑functional teams and represents clinical pharmacology in regulatory interactions to enable efficient, data‑driven advancement of therapies across our neuroscience portfolio.

Key Responsibilities

Lead clinical pharmacology strategy for CNS and neuroscience programs from first‑in‑human through registrational and post‑marketing stages Design, execute, and interpret clinical pharmacology studies, including FIH, multiple‑ascending dose, DDI, biopharmaceutics, and patient studies Drive dose selection and optimization using integration of PK, PD, safety, efficacy, and CNS‑specific biomarkers Lead model‑informed drug development, including population PK, PK/PD, and exposure–response analyses relevant to CNS targets Assess and guide strategies for CNS exposure, brain penetration, target engagement, and translational biomarkers Serve as the clinical pharmacology lead on program teams, clinical sub‑teams, and trial working groups Author and oversee clinical pharmacology sections of regulatory documents (e.g., INDs, CTAs, IBs, NDAs) Represent clinical pharmacology in interactions with FDA and other global health authorities, supporting dose justification and labeling discussions Partner closely with DMPK, Translational Sciences, Clinical Development, Biomarkers, Biostatistics, CMC, and Regulatory Affairs Oversee CROs and external vendors conducting clinical pharmacology and modeling activities Ensure timely communication and clear interpretation of clinical pharmacology results to internal stakeholders Contribute to portfolio strategy, program prioritization, and long‑range clinical development planning for CNS assets Serve as a subject‑matter expert on clinical pharmacology considerations unique to neuroscience drug development Mentor and develop clinical pharmacology talent as the pipeline and organization grow Ensure high‑quality, submission‑ready documentation aligned with global regulatory standards

Qualifications

PharmD or a PhD in Clinical Pharmacology, Pharmacokinetics, Pharmaceutical Sciences, or a related discipline 12+ years of experience in clinical pharmacology within biopharma, with demonstrated impact in clinical drug development Extensive experience developing and executing clinical pharmacology strategies for early‑ through late‑stage programs, including registrational support Strong expertise in PK, PD, PK/PD integration, exposure–response analyses, and drug–drug interaction assessment Demonstrated experience applying quantitative clinical pharmacology approaches (e.g., population PK, mechanistic PK/PD modeling) to inform CNS dose selection and optimization Proficiency with clinical pharmacology tools and platforms such as NONMEM, R, Phoenix WinNonlin, SimCyp, or equivalent Experience authoring and delivering clinical pharmacology components of regulatory submissions (e.g., INDs, CTAs, NDAs) and interacting with global health authorities Strong understanding of translational PK, CNS exposure considerations, and biomarker integration in neuroscience drug development Excellent communication, collaboration, and leadership skills with the ability to operate effectively in a fast‑paced, matrixed environment

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Compensation

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within this range will be determined based on a variety of factors, including