Director, Pharmacoepidemiology & External Partnerships

Regeneron Pharmaceuticals, Inc; United States; On-site; USD 180,000 - 240,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Director-level Pharmacoepidemiologist to lead strategy for real-world evidence and post-marketing studies, aligning with Global Clinical Development to accelerate regulatory filings.

The role requires strategic thinking, collaboration, and strong epidemiology expertise to influence decisions across functions. You will partner with GPS, Safety, Clinical Science and Regulatory Affairs to design studies, manage vendors, and develop SOPs while advancing

Qualifications

• A results-oriented, collaborative style.
• Ability to build consensus with leaders and colleagues to gain support for initiatives.
• Proven track record of developing and maintaining relationships with partners at all levels of the organization.
• Previous experience in and deep understanding of the drug development process.
• Ability to manage and prioritize multiple tasks and projects within a matrix organization.

Responsibilities

• Develop pharmacoepidemiology strategy for real-world evidence and post-marketing studies for regulatory filings.
• Collaborate with GPS Leads, Safety Scientists, Clinical Scientists, Regulatory Affairs to design and analyze studies.
• Represent Pharmacoepidemiology on cross-functional teams and external partnerships.
• Lead SOPs and process improvements; support regulatory filings and safety oversight.
• Manage contractors and external vendors; build relationships with external experts.

Skills

Collaborative style

Consensus building

Relationship management

Drug development knowledge

Project prioritization

Communication skills

Education

Bachelor's degree in Biotech/Pharma related field

Job description

Regeneron Pharmaceuticals, Inc. seeks a Director-level Pharmacoepidemiologist to lead strategy for real-world evidence and post-marketing studies, aligning with Global Clinical Development to accelerate regulatory filings.

The role requires strategic thinking, collaboration, and strong epidemiology expertise to influence decisions across functions. You will partner with GPS, Safety, Clinical Science and Regulatory Affairs to design studies, manage vendors, and develop SOPs while advancing