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Senior Manager, Clinical Diagnostics CDx (Precision Medicine)


Job Location:

Warren, OH - USA

Monthly Salary: $ 150500 - 245500
Posted: 12 June 2026 (30+ days ago)
Application Deadline: 29 October 2026
Vacancies: 1 Vacancy
The job posting is outdated and position may be filled

Job Summary

Build our future together:

At Regeneron we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Clinical Diagnostics to support end-to-end companion diagnostics (CDx) strategy and execution across our therapeutic this role you will translate scientific needs into fit-for-purpose assays for global decisions owning programs from feasibility through validation registration launch and post-market sustainment while partnering with biomarker clinical regulatory commercial and IVD collaborators.

This position offers the opportunity to contribute to a fast-growing science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Tarrytown NY

  • Work model/flexibility: Onsite

  • Travel percentage: Up to 5-10% for partner meetings clinical site visits and regulatory interactions.

Discover your role:

  • Execute end-to-end CDx strategy aligning diagnostic milestones with therapeutic clinical development and regulatory timelines

  • Lead cross-functional teams integrate workstreams clear obstacles and provide transparent status reporting to governance bodies and senior leadership

  • Manage IVD partners negotiating scope timelines budgets and quality and overseeing co-development and Joint Steering Committees

  • Define assay intent and contribute to target product profiles for CDx platforms (e.g. NGS PCR IHC Immunoassays) driving analytical and clinical validation

  • Embed CDx assays in trials with clinical teams covering screening/stratification sampling site readiness and lab operations

  • Partner with IVD Regulatory on global submissions (FDA EU IVDR PMDA) supporting pre-subs labeling and responses

  • Ensure compliance with quality and regulatory frameworks (ISO 13485/14971 CLSI IVDR GCP) maintaining documentation and audit readiness

  • Thrive in a fast-paced multi-tasking environment bringing strong communication skills to cross-functional collaboration.

This role requires:

  • Advanced degree in molecular biology pathology biomedical engineering or equivalent experience

  • 4 years in diagnostics development including 2 years leading CDx/IVD programs in pharma or diagnostics organizations

  • Proven delivery of CDx aligned to drug approvals with successful validation and regulatory submissions

  • Expertise in NGS PCR IHC and immunoassays along with validation standards and quality systems

  • Strong grasp of global regulatory pathways (FDA CDRH EU IVDR PMDA) for CDx labeling

  • Excellent communication leadership and stakeholder management skills with the ability to deliver clear updates to executive audiences

Does this sound like you Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race color religion or belief (or lack thereof) sex sexual orientation gender identity or expression gender reassignment marital or civil partnership status civil status pregnancy or parental status age disability nationality citizenship status ethnic or national origin membership of the Traveler community familial status genetic information military or veteran status or any other characteristic protected under applicable law. Where required we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process unless such accommodation would impose undue hardship.

Where necessary we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment specific role level and your skills and some countries collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include depending on country and role: annual bonuses or other incentive plans equity awards pension or retirement benefits 401(k) company match health and wellness programs fitness centers insurance benefits (e.g. medical dental vision life and disability) paid time off and family support benefits. For additional information about Regeneron benefits in the U.S. please visit For other locations additional information will be provided during the recruitment process. If you have any questions please speak with your recruiter.


Please be advised that at Regeneron we believe we do our best work when we are together. For that reason many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$150500.00 - $245500.00

Required Experience:

Senior Manager


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Discover how Regeneron (NASDAQ: REGN) harmonizes biology and technology to create life-changing medicines. Join our team and explore clinical trials.

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