Senior Director, Clinical Programs

🕒 May 26

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

GeneDx

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

At GeneDx, we believe that everyone deserves personalized, targeted medical care—and that it all begins with a genetic diagnosis. Fueled by one of the world’s largest rare disease data sets, our industry-leading exome and genome tests translate complex genomic data into clinical answers that unlock personalized health plans, accelerate drug discovery, and improve health system efficiencies. It all starts with a single test.

📋 Description

• Lead high-impact programs that advance GeneDx’s mission in rare disease diagnostics and precision medicine. • Direct program ownership as well as managing a team of clinical program managers. • Drive strategic initiatives within the Clinical Development team, including clinical research programs, medical input on product development, and regulatory support. • Support the design and execution of evidence generation strategies for established clinical programs. • Collaborate with internal partners to design and execute projects aligning with established clinical programs and evidence generation strategy. • Partner with internal and external stakeholders on prospective clinical and translational research efforts. • Oversee the development, review, and submission of scientific manuscripts, abstracts, posters, and other publications aligned with clinical programs. • Acts as a subject matter expert for rare diseases and genomic diagnostics for both internal teams and external stakeholders. • Lead and mentor clinical program managers, including resource allocation, coaching, and performance feedback.

🎯 Requirements

• PhD, MD (or equivalent) with board certification by the American Board of Medical Genetics and Genomics (or equivalent) required • 10+ years of experience in a clinical laboratory or industry role as a board certified ABMGG fellow required • 5+ years of experience in a medical affairs or clinical development role required • 5+ years of experience leading research efforts related to molecular diagnostics in rare diseases required • Strong level of clinical genetics knowledge in rare diseases • Strong publication record • Ability to work cross-functionally with other teams and external collaborators to drive strategic initiatives forward • Experience working with rare disease biopharma preferred • Experienced in solving complex problems and negotiating business deals • Excellent written and verbal communication skills • Exceptional presentation and public speaking skills • Ability to work independently and manage time effectively • Detail-oriented with strong organizational skills • Proven experience leading teams and managing cross-functional collaborators to deliver on goals of projects and programs • Proficient in working with databases and Microsoft Office Suite.

🏖️ Benefits

• Paid Time Off (PTO) • Health, Dental, Vision and Life insurance • 401k Retirement Savings Plan • Employee Stock Purchase Plan • Employee Discounts • Voluntary benefits • Programs for parents and parents-to-be