Director, Quantitative Clinical Pharmacology: PK/PD Modeling & Strategy

Sarepta Therapeutics; Rhode Island; Hybrid; USD 186,000 - 232,000; Full time

Job summary

Sarepta Therapeutics invites applications for the Director of Quantitative & Clinical Pharmacology. Lead pharmacology deliverables from early to late-stage development, focusing on dose selection, PK/PD modeling, and translational approaches.

This highly visible role involves collaboration with cross-functional teams and global regulatory engagements. The position is hybrid, on-site at Sarepta facilities in the United States, with expected leadership across clinical pharmacology strategy and

Qualifications

• PhD in Pharmaceutical Sciences, mathematics/engineering or related field with 7+ years experience in clinical pharmacology or pharmacometrics.
• Strong understanding of clinical pharmacology principles and PK/PD modeling.
• Experience with regulatory interactions.

Responsibilities

• Drives development and execution of quantitative pharmacology strategies across all stages of drug development through product registration.
• Leads clinical pharmacology expertise in development strategies, protocol preparation, study execution and data review.
• Performs model-based analyses including population PK, PK/PD modeling and simulation, meta-analysis and disease modeling.

Skills

PK/PD modeling

Population PK

Regulatory interactions

Communication

Clinical pharmacology

Education

PhD in Pharmaceutical Sciences or related field

Tools

NONMEM

R

Job description

Why Sarepta? Why Now?

The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.

We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.

What Sarepta Offers

At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:

• Physical and Emotional Wellness

• Financial Wellness

• Support for Caregivers
  

For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us

The Importance of the Role

The Director of Quantitative & Clinical Pharmacology will be responsible to lead clinical pharmacology and pharmacometrics deliverables from early through late-stage clinical development (Ph3 and product registration), with an emphasis on clinical dose selection/refinement and predictive PK/PD modeling inclusive of population and statistically-based methodologies, as well as mechanistic and translational-focused approaches. This is a highly visible and team-facing role.

The Opportunity to Make a Difference

• Drives the development and execution of the quantitative pharmacology strategies across all stages of drug development through product registration
• Leads clinical pharmacology expertise in clinical and translational development strategies, protocol preparation, study execution, data review/analysis, study reports

• Responsible for model-based data analyses including population PK, PK/PD modeling and simulation, meta-analysis, disease modeling to inform clinical development
• Serves as functional lead for global regulatory strategies and HA engagements

• Maintains leading-edge knowledge in clinical pharmacology and pharmacometrics discipline, publishes manuscripts, presents at scientific conferences and scientific forums.

More about You

• PhD in Pharmaceutical Sciences, mathematics/engineering or related field with 7 years of experience working in clinical pharmacology or pharmacometrics

• Strong understanding of clinical pharmacology principles, strong hands-on experience with PK/PD modeling analysis, and experience in regulatory interactions

• Excellent communication, multitasking, and collaboration skills
• Experience in NONMEM & R highly preferred
• siRNA and/or CNS experience is preferred

What Now?

We're always looking for solution-oriented, critical thinkers.

So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.

#LI-HybridThis position is hybrid, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time.

The targeted salary range for this position is $185,600 - $232,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.