Director, Clinical Pharmacology

United States·WalthamFull-timeexecutive

OtherDirectorHealthcare

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Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies either as single agents or as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.

We are seeking a Director, Clinical Pharmacology will be responsible for developing and implementing clinical pharmacology and modeling & simulation strategies to support Crescent’s research and development programs. The ideal candidate will provide expertise in pharmacokinetics, dose optimization, pharmacometrics, collaborate with cross-functional teams and manage clinical pharmacology activities, data analysis, and global regulatory filings.

Serve as the lead clinical pharmacologist on the project team, accountable for clinical pharmacology deliverables, providing subject matter expertise on PK/PD and quantitative pharmacology.

Play a pivotal role in planning and executing clinical pharmacology activities to support development programs.

Drive utilization of model-based drug development approach for human PK prediction, dose and dosing regimen selection and optimization, collaborating closely with cross functional colleagues.

Oversee and/or perform PK/PD data analyses and contribute to the interpretation of study results through all phases of clinical development.

Lead preparation and review of clinical pharmacology sections of study protocols, reports, investigators' brochures and regulatory filings (IND’s, BLA’s, etc.), and respond to regulatory inquiries related to clinical pharmacology.

Provide oversight to vendors and consultants to ensure timely delivery of high-quality data and reports to support go/no-go decisions and dosing strategy.

Assure the implementation and adherence to SOPs, GXPs, and regulatory standards in clinical pharmacology programs.

PhD in pharmaceutical sciences, pharmacology with a focus on pharmacokinetics and pharmacometrics.

Strong understanding of clinical pharmacology study design, data analysis, and regulatory requirements.

Minimum 8 years of experience in clinical pharmacology and pharmacometrics, with hands-on experience in PK data analysis.

Prior experience in the field of ADC development is a plus.

Experience in the Oncology therapeutic area is highly desirable.

Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment

Competitive compensation, including base salary, performance bonus, and equity

100% employer-paid benefits package

Flexible PTO; also, two, one-week company-wide shutdowns each year

A commitment to your professional development, with access to resources, mentorship, and growth opportunities

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