Senior CDM Program Lead — Associate Director (Hybrid)

Regeneron Pharmaceuticals, Inc.; Kentucky; Hybrid; USD 157,000 - 257,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking an Associate Director, Clinical Data Management, Program Lead to steer the strategic CDM activities across assigned clinical programs.

You will ensure quality, timelines, and budgets while collaborating with senior leadership, study teams, vendors, and partners. You will provide CDM expertise during protocol design, study start-up, and conduct, promote standards, oversee timelines and budgets, and mentor team members in a matrix environment.

Qualifications

• Leadership and strategic CDM oversight experience.
• Strong project management and communication skills.
• Ability to guide protocol design and study start-up with CDM input.

Responsibilities

• Lead the overall success of CDM deliverables across studies and programs.
• Communicate program status, risks, and issues to collaborators and develop mitigation strategies.
• Provide CDM expertise during protocol design, study start-up, and study conduct, promoting standards.

Skills

Leadership

Project management

Communication

Mentorship

Education

Bachelor's degree in Mathematics, Science, or related field

Tools

21 CFR Part 11

ICH-GCP

CDISC standards

Job description

Regeneron Pharmaceuticals, Inc. is seeking an Associate Director, Clinical Data Management, Program Lead to steer the strategic CDM activities across assigned clinical programs.

You will ensure quality, timelines, and budgets while collaborating with senior leadership, study teams, vendors, and partners. You will provide CDM expertise during protocol design, study start-up, and conduct, promote standards, oversee timelines and budgets, and mentor team members in a matrix environment.