
1001 - 5000 Mitarbeiter
Bei GeneDx sind wir der Überzeugung, dass jeder eine personalisierte, zielgerichtete medizinische Versorgung verdient – und dass alles mit einer genetischen Diagnose beginnt. Angetrieben von einem der weltweit größten Datensätze seltener Krankheiten, übersetzen unsere branchenführenden Exom- und Genom-Tests komplexe genomische Daten in klinische Antworten, die personalisierte Gesundheitspläne ermöglichen, die Wirkstoffentdeckung beschleunigen und die Effizienz des Gesundheitssystems verbessern. Alles beginnt mit einem einzigen Test.
🕒 vor 17 Tagen
🗣️🇺🇸🇬🇧 Englisch erforderlich
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1001 - 5000 Mitarbeiter
Bei GeneDx sind wir der Überzeugung, dass jeder eine personalisierte, zielgerichtete medizinische Versorgung verdient – und dass alles mit einer genetischen Diagnose beginnt. Angetrieben von einem der weltweit größten Datensätze seltener Krankheiten, übersetzen unsere branchenführenden Exom- und Genom-Tests komplexe genomische Daten in klinische Antworten, die personalisierte Gesundheitspläne ermöglichen, die Wirkstoffentdeckung beschleunigen und die Effizienz des Gesundheitssystems verbessern. Alles beginnt mit einem einzigen Test.
• 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.
• 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.
• 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
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