Endocrinology Medical Director, Clinical Trials Leader

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

Benefits offered by this job

Annual bonuses

Equity awards

Pension or retirement benefits

401(k) company match

Health and wellness programs

Fitness centers

Insurance benefits (medical, dental, <

Paid time off

Family support benefits

Job summary

Regeneron Pharmaceuticals is seeking a Medical Director to lead the Endocrinology clinical development program, driving study concepts and protocols with cross-functional teams. You will oversee patient safety, data reviews, and publications while shaping strategic development opportunities in rare diseases.

Ideal candidates hold an MD with Endocrinology certification, have 2+ years pharma experience, and demonstrate strong regulatory collaboration abilities.

Qualifications

• MD or equivalent required; board eligibility or board certification in Endocrinology strongly preferred
• At least 2 years pharmaceutical industry experience (academic research acceptable)
• Experience in rare disease drug development strongly preferred
• Interactions with regulatory agencies or CTD/dossier submissions in an ICH region are an advantage

Responsibilities

• Guide Global Clinical Study Team to deliver high-quality trials on time
• Oversee medical monitoring of trials to ensure patient safety and regulatory compliance
• Lead clinical study and protocol development and present to stakeholders
• Provide clinical and scientific leadership for data review, study reports and publications
• Collaborate with cross-functional partners to advance program goals and deliverables
• Partner with discovery teams to shape future targets and development opportunities

Skills

Endocrinology expertise

Clinical trial leadership

Regulatory knowledge

Pharma industry experience

Education

MD degree

Job description

Regeneron Pharmaceuticals is seeking a Medical Director to lead the Endocrinology clinical development program, driving study concepts and protocols with cross-functional teams. You will oversee patient safety, data reviews, and publications while shaping strategic development opportunities in rare diseases.

Ideal candidates hold an MD with Endocrinology certification, have 2+ years pharma experience, and demonstrate strong regulatory collaboration abilities.