Regeneron
Healthcare & Life SciencesDirect Workday career site

Associate Director Precision Medicine - Clinical Diagnostics

Pay
$176,100 – $287,300 per year
Location
Remote (US)
Job type
Full-time
Level
Director
Experience
8+ years
Education
Doctorate
Listed
22 days ago

Skills & highlights for this role

  • CDx regulatory pathways
  • companion diagnostics
  • biomarker strategy
  • assay validation
  • FDA CDRH regulatory pathways

Also useful

  • NGS
  • PCR
  • immunohistochemistry

Stated benefits & perks

  • Health

About the role

Build our future together: We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution.

This role owns companion diagnostic programs from early biomarker feasibility through clinical validation, regulatory submission, and launch - translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions.

You'll work at the interface of biomarker science, clinical development, regulatory, and external IVD partners to ensure diagnostics keep pace with therapeutic milestones.

When & where: Location: Remote, USA Discover your role: Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles, defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays).

Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics. Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints.

Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment.

Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs.

This role requires: PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. 8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. Track record translating biomarker science into validated assays supporting drug approvals.

Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). Ability to translate complex scientific and clinical data for cross-functional and executive audiences. Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. #PrecisionMedicineCDX 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. 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 experience. In 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 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 on-site.

Please speak with your recruiter and hiring manager for more information about on-site 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) $176,100.00 - $287,300.00

Read the original posting

From Regeneron's careers page, first listed on Rolev.ai on October 19, 2026. Rolev.ai is not the employer.

How Rolev.ai helps with this application

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Common questions

What is the salary for the Associate Director Precision Medicine - Clinical Diagnostics role at Regeneron?

The Associate Director Precision Medicine - Clinical Diagnostics posting at Regeneron states compensation of $176,100 – $287,300 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Regeneron's official career site.

Where is the Associate Director Precision Medicine - Clinical Diagnostics job at Regeneron located?

Yes, this Associate Director Precision Medicine - Clinical Diagnostics opening at Regeneron is listed as Remote (US). Always check Regeneron's application page for specific state eligibility or relocation policies.

What qualifications are required for Associate Director Precision Medicine - Clinical Diagnostics at Regeneron?

For the Associate Director Precision Medicine - Clinical Diagnostics role, Regeneron highlights 8+ years of relevant experience; a doctorate; experience with companion diagnostics, biomarker strategy, assay validation, FDA CDRH regulatory pathways. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.

How do I apply for the Associate Director Precision Medicine - Clinical Diagnostics position at Regeneron?

This listing links directly to Regeneron's Workday application page. You can apply directly on Regeneron's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.