Associate Director, Clinical Pharmacology (Oncology)

Regeneron Pharmaceuticals

1d • $176,100 - $287,300 • Onsite

About The Position

We are looking for an Associate Director, within our Clinical Pharmacology group. Providing strategic and scientific expertise, as well as representing Clinical Pharmacology at relevant meetings. This position will provide CP subject matter support to new and on-going clinical programs primarily in the Oncology area. This role must be onsite 4-days per week at either our Tarrytown, NY, Warren, NJ or Cambridge, MA location. We offer a comprehensive relocation package. A day in the life an Associate Director may look like: Proactively-identify and provide significant PMx contributes 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 regarded as an expert in the field; as such is able to contribute to the overall strategic program development and is able to communicate complex PMx strategies and results in an influential manner to the development team. Independently designs and conducts or otherwise oversees the development of PMx analysis plans and applies standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses. Informs PMx management of results and issues in a timely manner. Advanced knowable of the field and know willingness to provide mentorship, is regarded as a scientific leader in PMx. Responsible for the preparation and timely delivery of accurate and well-articulated nonclinical or clinical study reports and regulatory submission documents as appropriate.

Requirements

• A PhD, Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.), Medicine (MD)
• At least 6+ years of relevant Clinical Pharmacology experience.

Nice To Haves

• Oncology experience is strongly preferred

Responsibilities

• Proactively identify and provide significant PMx contributions 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.
• Contribute to the overall strategic program development and communicate complex PMx strategies and results in an influential manner to the development team.
• Independently design and conduct or otherwise oversee the development of PMx analysis plans and apply standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses.
• Inform PMx management of results and issues in a timely manner.
• Provide mentorship and be regarded as a scientific leader in PMx.
• Responsible for the preparation and timely delivery of accurate and well-articulated nonclinical or clinical study reports and regulatory submission documents as appropriate.

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree