Senior Director, Clinical Pharmacology
About this opportunity
Job Summary:
The Senior Director, Clinical Pharmacology provides clinical pharmacology leadership across development programs, directing PK/PD strategy, modeling and simulation, and dose-selection activities to inform clinical trial design and regulatory submissions. Leads population PK, exposure-response, and other quantitative modeling efforts performed internally or through modeling vendors and translates the resulting insights into dose-selection rationale that shapes protocol design. Serves as the clinical pharmacology voice on cross-functional program teams and represents the function directly with health authorities during meetings and submission reviews. This role requires both technical modeling expertise and the credibility to defend clinical pharmacology strategy in high-stakes regulatory interactions.
Work Arrangement & Location:
Hybrid - This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week, currently designated as Tuesday and Wednesday. Additional on-site days may be required based on business needs, team priorities, or leadership direction.
Essential Duties and Responsibilities:
Lead clinical pharmacology strategy for assigned programs, including PK/PD study design and dose-selection rationale.
Direct population PK, exposure-response, and modeling and simulation analyses performed internally or by vendors.
Author and review clinical pharmacology sections of INDs, NDAs/BLAs, and health authority responses.
Serve as clinical pharmacology lead on cross-functional program teams, advising on drug-drug interaction and special population studies.
Represent clinical pharmacology in interactions with health authorities (e.g., FDA/CHMP meetings), including authorship of relevant sections of briefing documents.
Provide clinical pharmacology assessments to due diligence and licensing evaluations, as applicable.
Oversee clinical pharmacology CRO and modeling vendor relationships and deliverables.
Perform other duties and responsibilities as assigned
Qualifications:
Education: PharmD, PhD in Clinical Pharmacology, Pharmacokinetics, Pharmacometrics, pharmaceutical sicences, or related discipline required.
10+ years of clinical pharmacology experience in pharma/biotech, including leadership of PK/PD strategy across development-stage programs.
3+ years of vendor management oversight experience with ability to manage and hold CRO/modeling vendors accountable for deliverable quality.
Experience in immunology, inflammation, autoimmune disease, immune-mediated diseases, T-cell biology, cell therapy, biologics, gene therapy, or other novel therapeutic modalities preferred
Expertise in population PK/PD modeling, , and relevant software (e.g., NONMEM, R).
Strong knowledge of ICH and FDA/EMA clinical pharmacology guidance.
Understanding of drug-drug interaction and special population study design.
Proven ability to lead clinical pharmacology strategy discussions with senior internal and external stakeholders, including regulators.
Excellent scientific writing and presentation skills for regulatory submissions and health authority interactions.
Skilled at defending clinical pharmacology strategy directly with health authorities.
Demonstrated ability to manage external CROs/vendors and coordinate study execution across multiple stakeholders
Strong project/program management capability, including timeline planning, cross-functional coordination, risk tracking, deliverable management, and issue escalation.
Ability to communicate scientific and operational issues clearly to cross-functional teams and senior stakeholders.
Salary Range:
The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.
Salary Range
$266,000, $344,000 USD
Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 301 comparable Senior Director Clinical Development roles across 51 biopharma companies.
Salary context
165 of 301 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 301 comparable roles
+ 10 more countries
Seniority mix
301 of 301 peers have a known seniority level
Therapeutic area mix
105 of 301 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.