Senior Director, Quantitative Pharmacology

Regeneron Pharmaceuticals • Cambridge, MA

205d • $238,400 - $397,300

About The Position

As a Senior Director in Pharmacometrics, this individual will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio. In this capacity, the Senior Director is accountable for the successful and timely completion of all assignments encompassing a broad array of deliverables in support of the corporate strategic goals. The Senior Director is expected to apply both logistical and strategic initiatives as well as to incorporate novel and creative scientific approaches. A typical day in this role might look like: Utilizing a mastery level of PK/PD knowledge and strategic leadership skills, effectively develop and implement strategic analyses in support of research and development projects. Adapts plans and priorities that address resource and operational challenges. Accountable for the appropriate application of PMx and corporate policies and procedures. May provide technical guidance and mentoring of colleagues within the function and across the organization. Accountable for the PK/PD evaluation of a portfolio of products or projects, and/or highly complex projects that are wide in scope. Anticipates and assesses internal and/or external business, scientific and/or regulatory challenges; and is able to recommend sound solutions. Finds opportunities for process and improvements, product or service improvements. Solves unique and complex problems that have a broad impact on the business. Influential across the organization to include individual contributors (in and out of the function), development program teams, and other functional managers.

Requirements

• Advanced education in the sciences and pharmaceutical industry experience.
• Mastery in the field and recognized as an expert within the organization and externally.
• Demonstrated significant impact on the organization and ability to influence change.
• Strong collaborative skills and effective at building alliances across functions.
• Ability to influence colleagues and multi-disciplinary project teams.
• Experience handling complex projects with considerable ambiguity.
• Good mentoring skills and ability to identify business problems and craft solutions.
• Ability to engage with regulatory agencies and develop regulatory strategy.

Nice To Haves

• Active professional representation of the company externally.
• Leadership in cross-functional process initiatives.
• Experience working with senior management on solving issues.

Responsibilities

• Manage PMx support for various programs in therapeutic focus areas.
• Develop and implement strategic analyses for research and development projects.
• Adapt plans and priorities to address resource and operational challenges.
• Ensure appropriate application of PMx and corporate policies and procedures.
• Provide technical guidance and mentoring to colleagues.
• Accountable for PK/PD evaluation of products or projects.
• Anticipate and assess business, scientific, and regulatory challenges; recommend solutions.
• Identify opportunities for process and product improvements.
• Solve complex problems impacting the business.
• Influence across the organization, including development program teams.

Benefits

• Health and wellness programs
• Fitness centers
• Equity awards
• Annual bonuses
• Paid time off for eligible employees

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Industry: Chemical Manufacturing
• Education Level: Master's degree
• Number of Employees: 5,001-10,000 employees