... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
... owning programs from feasibility through validation, registration, launch, and post-market ... CDx labeling * Excellent communication, leadership, and stakeholder management skills, with the ...
You will own programs from feasibility through analytical/clinical validation, registration, launch ... CDx labeling. * Excellent communication, leadership, and stakeholder management; clear, concise ...
You will own programs from feasibility through analytical/clinical validation, registration, launch ... CDx labeling. * Excellent communication, leadership, and stakeholder management; clear, concise ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $131K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $131K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $130K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $130K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
As the Staff Program Manager, you will be accountable for moving programs from opportunity assessment and partner agreement through assay development, clinical and analytical validation, regulatory ...
As the Staff Program Manager, you will be accountable for moving programs from opportunity assessment and partner agreement through assay development, clinical and analytical validation, regulatory ...
As the Staff Program Manager, you will be accountable for moving programs from opportunity assessment and partner agreement through assay development, clinical and analytical validation, regulatory ...
As the Staff Program Manager, you will be accountable for moving programs from opportunity assessment and partner agreement through assay development, clinical and analytical validation, regulatory ...
As the Staff Program Manager, you will be accountable for moving programs from opportunity assessment and partner agreement through assay development, clinical and analytical validation, regulatory ...
As the Staff Program Manager, you will be accountable for moving programs from opportunity assessment and partner agreement through assay development, clinical and analytical validation, regulatory ...
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $131K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... across molecular programs and strategic campaigns. Foster an inclusive culture of scientific ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $131K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... across molecular programs and strategic campaigns. Foster an inclusive culture of scientific ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $130K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Director, CDx & Clinical Platform Development
South San Francisco, CA · On-site
$96K - $130K/yr
Cultivate and manage critical strategic alliances with internal and external regulatory and policy ... programs and strategic campaigns. * Foster an inclusive culture of scientific excellence ...
Manage the full sales cycle: first contact through contract execution and initial account handover ... program needs. * Work cross‑functionally with legal, finance, and lab operations to align on ...
Manage the full sales cycle: first contact through contract execution and initial account handover ... program needs. * Work cross‑functionally with legal, finance, and lab operations to align on ...
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 ...
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 ...
Associate Director, Precision Medicine (Clinical Diagnostics)
Armonk, NY · On-site
$176K - $287K/yr
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 ...
Associate Director, Precision Medicine (Clinical Diagnostics)
Armonk, NY · On-site
$176K - $287K/yr
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Cdx Program Manager information
See salary details
$68.5K - $74.7K
0% of jobs
$74.7K - $80.9K
0% of jobs
$80.9K - $87K
0% of jobs
$87K - $93.2K
0% of jobs
$93.2K - $99.4K
0% of jobs
$99.4K - $105.6K
1% of jobs
$105.6K - $111.8K
8% of jobs
$113.3K is the 25th percentile. Wages below this are outliers.
$111.8K - $118K
61% of jobs
$120.4K is the 75th percentile. Wages above this are outliers.
$118K - $124.1K
10% of jobs
$124.1K - $130.3K
0% of jobs
$130.3K - $136.5K
19% of jobs
$68.5K
$118.9K
$136.5K
How much do cdx program manager jobs pay per year?
What is a CDx program manager?
What are some common challenges faced by a CDx program manager when coordinating cross-functional teams?
What are the key skills and qualifications needed to thrive as a CDx program manager, and why are they important?
What is the difference between Cdx Program Manager vs Cdx Project Coordinator?
| Aspect | Cdx Program Manager | Cdx Project Coordinator |
|---|---|---|
| Credentials | Bachelor's degree; PMP or similar certifications often preferred | Bachelor's degree; certifications like CAPM beneficial |
| Work Environment | Oversees multiple projects, strategic planning, stakeholder communication | Supports project teams, manages schedules, assists with project tasks |
| Industry Usage | Common in technology, manufacturing, and logistics sectors | Frequent in similar industries, supporting project execution |
The Cdx Program Manager focuses on strategic oversight and managing multiple projects, while the Cdx Project Coordinator handles day-to-day project support and coordination. Both roles require similar credentials but differ in scope and responsibilities, with the Program Manager playing a more leadership-oriented role.
Is a CDX Program Manager a stressful job?
What are popular job titles related to Cdx Program Manager jobs?
For Cdx Program Manager jobs, the most frequently searched job titles are:

Senior Manager, Clinical Diagnostics CDx (Precision Medicine)
Warren, NJ
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted yesterday
Regeneron rating
8.6
Based on 45 frontline employees who took The Breakroom Quiz
Job description
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 indications. In 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 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 additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. 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)
$150,500.00 - $245,500.00What Regeneron employees say
Pay
Benefits
Hours and flexibility
Workplace
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About Regeneron
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
5,001 - 10,000 Employees
Headquarters location
Tarrytown, NY, US
Year founded
1988