Associate Director Clinical Pharmacology

Regeneron Pharmaceuticals, Inc; Cambourne; On-site; GBP 105,000 - 150,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks an Associate Director for its Clinical Pharmacology group. The role demands strategic and scientific leadership in oncology programs, with responsibility for PK/PD analyses and regulatory submissions.

You will mentor more junior staff and present complex results to development teams. The position emphasizes cross-functional collaboration and influence across programs, with onsite work four days per week at our sites in the US.

Qualifications

• PhD and 8+ years of clinical pharmacology experience.
• Ability to mentor and guide teams across programs.
• Strong communication of complex strategies to development teams.

Responsibilities

• Provide strategic and scientific expertise for oncology programs.
• Lead or oversee PK/PD analyses and other quantitative analyses.
• Prepare timely clinical study reports and regulatory submission documents.
• Represent Clinical Pharmacology at relevant meetings and cross-functional teams.

Skills

Mentorship

Strategic communication

Cross-functional teamwork

Clinical pharmacology expertise

Education

PhD in Biology, Pharmacology, Engineering, Pharmacy or Medicine (MD) or Pharm.D.

Job description

Build our Future Together

We are looking for an Associate Director for our Clinical Pharmacology group. The incumbent will provide strategic and scientific expertise, as well as represent Clinical Pharmacology at relevant meetings. This position will provide Clinical Pharmacology subject matter support to new and on-going clinical programs primarily in the Oncology area.

When & where:

• Work Location: Tarrytown, NY, Warren, NJ, or Cambridge, MA
• Work model/flexibility: 4 days per week onsite

Discover your role:

• Proactively-identify and provide significant clinical pharmacology contributions, potentially of a complex nature, for research and development programs that address strategically important program needs, and that represent scientific advancements of one or more programs and/or aptly address significant regulatory hurdles.
• Is able to contribute to the overall strategic program development and is able to communicate complex strategies and results in an influential manner to the development team.
• Independently designs and conducts or otherwise oversees the development of analysis plans and applies standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses. Informs management of results and issues in a timely manner.
• Advanced knowledge of clinical pharmacology and willingness to provide mentorship, is regarded as a scientific leader in the field.
• Responsible for the preparation and timely delivery of accurate and well-articulated clinical study reports and regulatory submission documents.
• Ability to make a significant impact on the organization and external groups and can influence and effect change.
• Enjoy making contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.
• Wants to work in cross-functional teams with forward-thinking, passionate, and driven teammates.

This role requires:

• A PhD in Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.) or Medicine (MD)
• 8+ years of relevant Clinical Pharmacology experience