City Therapeutics Posted June 3, 2026

Associate Director, Clinical Pharmacology

Cambridge, Massachusetts, United States Type not listed
Clinical Development Associate Director
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City Therapeutics is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Associate Director, Clinical Pharmacology

City Therapeutics is advancing a next-generation platform for RNAi medicines designed to unlock the full therapeutic potential of gene silencing. By combining innovative delivery technologies with deep expertise in RNA biology, we are building a pipeline of transformative medicines for patients with serious diseases. We are seeking a highly motivated and scientifically rigorous Clinical Pharmacology Scientist to join our dynamic and growing Translational Sciences Team to help shape the clinical development strategy of our growing portfolio.

The Associate Director of Clinical Pharmacology will play a critical role in the design, execution, analysis, and interpretation of clinical pharmacology strategies across City Therapeutics' development programs. This individual will report to the Head of Clinical Pharmacology and Pharmacokinetics (CPPK), and provide scientific leadership for pharmacokinetic (PK), pharmacodynamic (PD), exposure-response, and dose selection activities from first-in-human studies through late-stage clinical development.

The successful candidate will work in a highly cross-functional environment, partnering closely with Clinical Development, Regulatory Affairs, Clinical Operations, Biostatistics, Data Science, CMC and external collaborators to drive data-driven decision making and advance clinical development.

 

Key Responsibilities

Lead development and execution of clinical pharmacology strategies for RNAi therapeutic clinical programs.

Lead and execute model-informed drug development (MIDD) activities, including population PK, exposure-response, PBPK, and mechanistic PK/PD modeling, either independently or in collaboration with quantitative scientists, to support regulatory interactions and development planning.

Contribute to clinical protocol design, statistical analysis plans, clinical study reports, and investigator brochures.

Author and review clinical pharmacology sections of regulatory documents including INDs, briefing packages, meeting requests, and marketing applications.

Participate in interactions with health authorities and contribute to regulatory strategy discussions.

Develop dose selection and dose optimization strategies to support clinical development and regulatory submissions.

Integrate nonclinical, translational, biomarker, PK/PD, and clinical data to inform clinical development decisions.

Review emerging clinical data and communicate pharmacology insights to project teams and senior leadership.

Ensure clinical pharmacology plans align with current regulatory expectations and industry best practices.

Qualifications

PhD, PharmD, MD, or equivalent advanced degree in Clinical Pharmacology, Pharmaceutical Sciences, Pharmacokinetics, Pharmacometrics, Biomedical Engineering, or a related discipline.

7+ years of relevant industry experience in clinical pharmacology or pharmacometrics.

Demonstrated experience supporting early and/or late-stage clinical development programs.

Experience leading clinical pharmacology activities across multiple development programs and regulatory interactions.

Hands-on experience with population PK modeling and exposure-response analyses for dose recommendation and optimization.

Experience working with external CROs and pharmacometric vendors.

Knowledge of regulatory expectations related to clinical pharmacology and model-informed drug development.

Experience contributing to CTA, IND, NDA, BLA, or equivalent regulatory submissions.

Excellent scientific communication and presentation skills.

Ability to influence cross-functional teams in a fast-paced biotechnology environment.

Prior participation in FDA, EMA, or other global regulatory agency interactions.

Familiar with translational biomarkers and precision medicine approaches.

Experience in oligonucleotide therapeutics, i.e. siRNA, antisense, gene editing, or other nucleic acid-based modalities.

Compensation

The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package. Pay range is $174,000 to $196,000

Why You’ll Love Working Here

At City, you’ll be part of a team that’s as ambitious as it is collaborative. We’re building an organization that is united by our values:

• Courage: We seek out the unknown, challenge boldly, and fight for patients.

• Innovation: Curiosity drives us to push the boundaries of what’s possible.

• Tempo: We move fast and with purpose. Patients can’t wait, and neither will we.

• Yes: We collaborate intensely, with candor and optimism, taking ownership and celebrating the journey together.

If you’re driven by discovery, pace, and purpose, welcome to City.

Our Working Model: In Person, By Design

At City, we believe that science and culture thrive together, and that happens best in person. Our working model is clear: we work onsite at our Kendall Square offices five days per week.

This choice reflects our belief that great science and cultures run on connection, fairness, and growth.

• Connection: Face time matters. Building an enduring biotech company is about people, science, and strategy. Working side by side sharpens ideas, accelerates feedback, and fuels innovation for patients.

• Fairness: One model for all. Every voice counts, and fairness depends on shared experience. We hold ourselves to one standard across all levels and functions.

• Growth: Learning moves faster in person. Growth comes from conversation, observation, and mentorship. We believe in developing talent, and that happens best when we’re together.

We also know that life isn’t always predictable. When individual needs arise, we’re flexible and supportive and work together to balance home life with life at City.

We believe diverse teams drive better science. We welcome applicants from all backgrounds and experiences who share our mission to bring transformative RNAi medicines to patients.

City Therapeutics is an Equal Opportunity and Affirmative Action employer. All qualified applicants will receive consideration without regard to race, color, religion, national origin, gender, gender identity or expression, sexual orientation, age, disability, veteran status, or any other characteristic protected by law.

City Therapeutics is accepting applications from direct candidates only. Agency inquiries or submissions will not be accepted at this time.

Job details

Seniority
Associate Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Cambridge, Massachusetts, United States
Employment type
Not listed

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 504 comparable Associate Director Clinical Development roles across 76 biopharma companies.

504Comparable roles tracked
474Currently active
76Companies hiring similar roles
45Countries represented

Salary context

146 of 504 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.

This roleSubject $174,000/yr – $196,000/yr
Lowest disclosed · Sr Site Activation Coordinator · IQVIA $35,800/yr – $102,000/yr
Highest disclosed · Sr Statistical Advisor · Gilead Sciences, Inc. $261,375/yr – $338,250/yr
Peer group range $68,900 – $299,813 (median $175,600)

Where these roles are based

Top locations among the 504 comparable roles

United States221
India73
United Kingdom28
China18
Poland16
Taiwan16

+ 39 more countries

Seniority mix

504 of 504 peers have a known seniority level

Manager250
Senior143
Associate Director111

Therapeutic area mix

45 of 504 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology25
Immunology10
Neuroscience5
Ophthalmology2
Dermatology & Aesthetics1
Rare Disease1
Respiratory1

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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.

60%similar
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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.

60%
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AstraZeneca · Wilmington, Delaware, United States of America · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.