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Cdx Diagnostics Jobs (NOW HIRING)

Revolution Medicines

Senior Program Manager

Redwood City, CA · Hybrid

$142K - $142K/yr

The ideal candidate is a strategic program management professional with deep experience leading cross-functional Companion Diagnostics (CDx) development activities supporting targeted oncology ...

Foresight Diagnostics

Program Manager

Boulder, CO · On-site +1

Projects and programs may include development, validation, and regulatory submission of diagnostic products; support of biopharma companion diagnostic (CDx) partnerships; and product sustainment and ...

Revolution Medicines

Senior Program Manager

Redwood City, CA · On-site

$142K - $142K/yr

The ideal candidate is a strategic program management professional with deep experience leading cross-functional Companion Diagnostics (CDx) development activities supporting targeted oncology ...

AstraZeneca

Director, Diagnostics

Boston, MA · On-site

Own clinical trial diagnostic strategy,including patient selection, biomarker-driven enrichment, and Companion Diagnostic (CDx) development,ensuringspeed ofenrollment, data quality, and regulatory ...

Foresight Diagnostics Inc.

Program Manager

Aurora, CO · On-site +1

Projects and programs may include development, validation, and regulatory submission of diagnostic products; support of biopharma companion diagnostic (CDx) partnerships; and product sustainment and ...

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Cdx Diagnostics information

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How much do cdx diagnostics jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for cdx diagnostics in the United States is $27.41, according to ZipRecruiter salary data. Most workers in this role earn between $22.60 and $31.73 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Cdx Diagnostics position, and why are they important?

To thrive as a professional in CDx Diagnostics, you need a strong background in laboratory science, molecular biology, or pathology, typically supported by relevant degrees and clinical laboratory certification. Familiarity with diagnostic testing platforms, specialized laboratory information systems (LIS), and regulatory compliance standards like CAP/CLIA is essential. Strong attention to detail, analytical thinking, and effective communication are important soft skills for collaborating with clinical teams and maintaining high-quality results. These skills are vital to ensure accurate diagnostic outcomes, regulatory adherence, and smooth interdisciplinary workflow in the healthcare setting.

What is a Cdx Diagnostics job?

A Cdx Diagnostics job typically involves working for a company that specializes in diagnostic testing, particularly for detecting precancerous and cancerous conditions in the gastrointestinal tract. Roles may include laboratory technicians, sales representatives, medical science liaisons, and customer support specialists. Employees often work with cutting-edge diagnostic technologies to support early disease detection and patient care. Responsibilities vary by position but generally include analyzing test results, collaborating with healthcare professionals, and ensuring regulatory compliance.

What does a typical day look like for someone working at CDx Diagnostics?

A typical day at CDx Diagnostics includes processing and analyzing clinical specimens, interpreting diagnostic results, and documenting findings in laboratory information systems. You will often collaborate closely with pathologists, lab technicians, and other clinical staff to ensure timely and accurate delivery of diagnostic data. The role involves a combination of hands-on laboratory work, data review, and communication with healthcare providers to aid in patient care. This dynamic environment encourages continual learning and offers opportunities for professional development through exposure to advanced diagnostic technologies.

More about Cdx Diagnostics jobs
What states have the most Cdx Diagnostics jobs? States with the most job openings for Cdx Diagnostics jobs include:
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Cdx Diagnostics jobs near you
Infographic showing various Cdx Diagnostics job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 98% Full Time, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $57,009 per year, or $27.4 per hour.
Senior Program Manager

Senior Program Manager

Revolution Medicines

Redwood City, CA • Hybrid

$142K - $142K/yr

Other

Posted 9 days ago

Job description

The Opportunity:

This is an exciting opportunity to advance first-in-Class RAS(ON) Inhibitors through clinical development.  The ideal candidate is a strategic program management professional with deep experience leading cross-functional Companion Diagnostics (CDx) development activities supporting targeted oncology therapies. This individual will drive alignment across internal functions and external diagnostic partners to enable successful clinical development, regulatory execution, and commercialization readiness. The successful candidate will draw on their experience to:

  • Lead cross-functional Companion Diagnostics development programs supporting clinical-stage oncology assets from assay strategy through clinical and regulatory execution.

  • Work closely with CDx Leads and other clinical development team members to facilitate science-based CDx decision making and drive the execution of the CDx development strategy.

  • Develop and maintain integrated cross-functional program plans, timelines, milestones, dependencies, and critical path analyses across internal teams and external diagnostic partners.

  • Drive cross-functional alignment and coordinate CDx operational activities across Translational Medicine, Clinical Development, Regulatory Affairs, Biomarker Sciences, Clinical Operations, Alliance Management, and external diagnostics partners and vendors.

  • Proactively identify program risks, resource constraints, and operational bottlenecks, and lead mitigation planning to ensure program execution and delivery.

  • Facilitate program governance activities, including preparation of executive-level updates, program status reporting, risk escalation, and decision tracking.

  • Partner with diagnostic partners and vendors and study teams to monitor execution against timelines, deliverables, and key milestones.

  • Lead implementation of program management best practices, operational processes, and scalable planning tools to support growing Companion Diagnostics capabilities.

  • Oversee implementation of clinical trial assays at reference labs and centralized testing vendors.

  • Support strategic planning activities related to Companion Diagnostics portfolio execution, regulatory readiness, and commercialization planning.

  • Influence cross-functional teams through data-driven recommendations, transparent communication, and structured problem-solving.

Required Skills, Experience and Education:

  • B.A. or BSc. In Life Sciences with 8+ years of biotechnology, pharmaceutical, diagnostics, or clinical development experience, including 5+ years leading cross-functional drug development or Companion Diagnostics programs.

  • Strong understanding of oncology drug development, biomarker strategy, assay development, clinical validation, and companion diagnostics regulatory pathways.

  • Demonstrated success in leading complex cross-functional initiatives in matrixed environments with internal and external stakeholders.

  • Strong strategic planning, risk management, and program governance skills.

  • Ability to influence stakeholders and drive alignment across multiple functions and organizational levels.

  • Excellent communication and executive presentation skills with the ability to synthesize complex information into actionable recommendations.

  • Experience developing integrated timelines, managing dependencies, and driving execution across multiple workstreams.

  • Strong motivation, attention to detail, ability to think independently and fully integrate into a high achieving team environment.

  • Highly proficient using MS Office, Lucid Charts and Project Management software to manage project timelines and resources (e.g. MS Project, Smartsheet, Office Timeline, etc.).

Preferred Skills:

  • MSc., MBA or advanced degree in related field preferred.

  • Experience managing Companion Diagnostics or biomarker-driven development programs.

  • PMP (Project Management Professional) or other PM certification or equivalent.

  • Experience in Oncology therapeutic area and clinical stages of drug development. 

    #LI-Hybrid #LI-EM1

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