Global Medical Lead, Endocrinology Trials

Regeneron Pharmaceuticals, Inc (USA); Washington (District of Columbia); On-site; USD 285,000 - 386,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

401(k) matching

Health benefits

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Medical Director to lead the Endocrinology clinical development program and serve as Medical Lead for trials, overseeing study concepts and protocols while collaborating with cross-functional teams.

The role requires an MD with endocrinology board eligibility or certification, plus at least 2 years of industry experience and rare disease development exposure. Regulatory interactions are valued.

Qualifications

• MD or equivalent with board eligibility or board certification in Endocrinology strongly preferred.
• At least 2 years pharmaceutical industry experience (or equivalent in academia).
• Experience in rare disease drug development strongly preferred.

Responsibilities

• Serve as Medical Lead for clinical trials and oversee study concepts and protocols.
• Oversee medical monitoring of trials to ensure patient safety and regulatory compliance.
• Lead clinical study and protocol development and present to internal/external stakeholders.
• Collaborate with cross-functional partners to advance program goals and deliverables.

Skills

Medical leadership

Clinical trial design

Regulatory knowledge

Endocrinology expertise

Education

MD or equivalent (Endocrinology board eligible/certified)

Job description

Regeneron Pharmaceuticals, Inc. seeks a Medical Director to lead the Endocrinology clinical development program and serve as Medical Lead for trials, overseeing study concepts and protocols while collaborating with cross-functional teams.

The role requires an MD with endocrinology board eligibility or certification, plus at least 2 years of industry experience and rare disease development exposure. Regulatory interactions are valued.