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Job type: Permanent

Discipline: Pharmacology

Location: United States

Head of Clinical Pharmacology - Permanent - Hybrid, Boston MA

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Primary Responsibilities:

The successful candidate will be required to serve as the functional leader of the Translational Pharmacology, Clinical Pharmacology, and Pharmacometrics functions of the company.

Your Profile:

We are looking for a candidate with:

D. or equivalent degree with at least 15 years of industry experience.
Educational background in PKPD, pharmacometrics, chemical engineering, biomedical engineering, biostatistics, or mathematics.
Prior experience working with monoclonal and multispecific antibodies; experience with ADCs is preferred.
Demonstrated strong technical expertise in quantitative approaches to translational pharmacology, early research, and clinical development.
Prior experience in using semi-/mechanistic modeling for target selection, target product profile optimization, and compound prioritization in early research.
Track record in using modeling and simulation approaches to support regulatory discussions and Biologics License Application (BLA) submissions.
Experience in Oncology.
Strong leadership skills with the ability to effectively influence cross-functional teams.
Strong work ethic, commitment to excellence, and openness to new ideas and feedback.

The Head of Clinical Pharmacology's responsibilities will be:

Serve as the functional leader of the Translational Pharmacology, Clinical Pharmacology, and Pharmacometrics functions of the company.
Be accountable for managing people, setting the strategic direction of the group, and allocating resources.
Collaborate with other functions to integrate quantitative approaches throughout the product lifecycle, enhancing technical success and decision-making confidence.
Partner with early research to provide foundational insights for optimization of key molecular attributes of monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs) to inform prioritization from product concept to preclinical optimization.
Collaborate closely with clinical stage project teams to provide scientific insights that drive clinical development decisions and support regulatory submissions.

Compensation:

$340,000 to $350,000 per annum.

If you are having difficulty in applying or if you have any questions, please contact Sofia Amark at s.amark@proclinical.com

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