Director, Quantitative Clinical Pharmacology PKPD Modeling & Strategy

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 2023 we launched our fourth therapy and the first ever gene therapy to treat Duchenne.

Were 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: 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

Were always looking for solution-oriented critical thinkers.

So if youre 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-Hybrid

This position is hybrid you will be expected to work on site at one of Sareptas 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 $185600 - $232000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sareptas 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.