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Companion Diagnostics Cdx Jobs (NOW HIRING)

BeiGene, Inc.

Director CDx Development

$176K - $236K/yr

The Companion Diagnostics (CDx) Lead will be responsible for defining and executing end-to-end diagnostic strategies that are fully aligned with clinical development programs and timelines. This role ...

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 ...

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Companion Diagnostics Cdx information

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How much do companion diagnostics cdx jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for companion diagnostics cdx in the United States is $15.05, according to ZipRecruiter salary data. Most workers in this role earn between $13.94 and $15.62 per hour, depending on experience, location, and employer.

What are some typical collaborations involved in a Companion Diagnostics (CDx) role, and how do these partnerships impact daily work?

Professionals in Companion Diagnostics (CDx) frequently collaborate with multidisciplinary teams that include clinical researchers, regulatory affairs specialists, laboratory scientists, and pharmaceutical partners. These collaborations are essential for aligning biomarker research with drug development timelines and ensuring regulatory compliance. Daily work often involves cross-functional meetings, data reviews, and joint problem-solving sessions to advance diagnostic assays in parallel with therapeutic candidates, making strong teamwork and communication skills crucial in this field.

What is the difference between Companion Diagnostics Cdx vs Laboratory Technician?

AspectCompanion Diagnostics CdxLaboratory Technician
Required CredentialsCertification in diagnostic or molecular testing, relevant degreesAssociate's or bachelor's in laboratory science or related field
Work EnvironmentPharmaceutical or biotech labs, hospitals, research facilitiesClinical or research laboratories, hospitals
Industry UsageDeveloping and validating diagnostic tests for targeted therapiesPerforming tests, preparing samples, maintaining lab equipment

Companion Diagnostics Cdx professionals focus on developing and validating diagnostic tests for personalized medicine, requiring specialized certifications. Laboratory Technicians perform routine testing and sample processing in clinical labs. While both roles work in laboratory settings, Cdx specialists are more involved in test development and validation, whereas technicians support daily testing operations.

What are companion diagnostics (CDx)?

Companion diagnostics (CDx) are medical devices, often in vitro tests, that provide essential information for the safe and effective use of a corresponding drug or biological product. They help identify patients who are most likely to benefit from a particular therapy or who may be at increased risk of adverse reactions. CDx tests are commonly used in personalized medicine, especially in oncology, to tailor treatments based on a patient's genetic or molecular profile. Their use can improve treatment outcomes and minimize unnecessary exposure to ineffective therapies.

What are the key skills and qualifications needed to thrive as a Companion Diagnostics (CDx) professional, and why are they important?

To thrive as a Companion Diagnostics (CDx) professional, you need a strong background in molecular biology, clinical research, and regulatory affairs, often supported by a degree in life sciences or related fields. Familiarity with diagnostic assay development, clinical trial management systems, and regulatory compliance tools such as FDA and EMA submissions is typical. Excellent project management, cross-functional collaboration, and communication skills distinguish top performers in this field. These skills are crucial to ensure the successful co-development of diagnostics and therapeutics, meeting regulatory standards and improving patient outcomes.
More about Companion Diagnostics Cdx jobs
What cities are hiring for Companion Diagnostics Cdx jobs? Cities with the most Companion Diagnostics Cdx job openings:
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Companion Diagnostics Cdx jobs near you
Infographic showing various Companion Diagnostics Cdx job openings in the United States as of July 2026, with employment types broken down into 13% Internship, 40% As Needed, 33% Full Time, 9% Temporary, 1% Contract, and 4% Nights. Highlights an 77% Physical, 7% Hybrid, and 16% Remote job distribution, with an average salary of $31,304 per year, or $15.1 per hour.

Senior Manager, Companion Diagnostics (CDx)

Tempus

Chicago, IL • On-site

$120K - $165K/yr

Full-time

Re-posted 3 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Senior Manager, Companion Diagnostics (CDx)
Tempus is seeking a Sr. Manager, Companion Diagnostics to lead the planning, oversight, and execution of complex Companion Diagnostic (CDx) clinical validation studies for our pharmaceutical partners. This is a critical, long-term resource needed to establish consistent, internal expertise for high-stakes CDx projects. This role will bridge the gap between drug trial requirements and diagnostic validation, ensuring regulatory compliance and timely study completion.
Key Responsibilities
  • Early Scoping & Alignment: Lead the initial scoping and planning of CDx validation projects and contracts, ensuring input from key internal experts, including Tempus Pharma sequencing, QA, CRO, and Regulatory, external IVD consultants, the drug trial sponsor, and others.
  • Protocol and Strategy Development: Lead the development of diagnostic protocols, including translating drug trial strategy into clinical Dx validation strategy, ensuring sound biostatistical approaches, and alignment on clinical data generation & analysis plans.
  • Cross-Functional Collaboration: Work in partnership with Tempus Pharma sequencing, QA, CRO, and Regulatory, external IVD consultants, the drug trial sponsor, and others to provide necessary input and oversight for both internal and external validation work.
  • Study Execution Oversight: Take ownership of the day-to-day management and execution of regulatory-grade CDx clinical studies for major partners.
  • Regulatory & Quality Compliance: Ensure all clinical validation activities meet the requirements for running clinical device studies, including adherence to GCP and regulatory scrutiny.
  • Project Management: Manage project deliveries, ensuring timely completion and appropriate resourcing to meet agreed-upon timelines.

Qualifications
  • A Ph.D. or Masters in a relevant discipline is highly preferred, though equivalent professional experience will be considered.
  • 5 years of demonstrated experience in IVD or medical device development with a minimum of 2 years of experience in clinical study design and execution.
  • Experience with GCP-grade study setup, monitoring, and reporting, including understanding of trial master file documentation and FDA strategies.
  • Proven ability to understand biostatistics strategy and help craft strategic workplans and Statistical Analysis Plans (SAPs) with support from SMEs (biostatistics, IVD consultants) as needed.
  • Familiarity with the distinct requirements and complexities of CDx clinical development, including clinical validation strategies and ensuring that studies are conducted and documented in accordance with good clinical practices and other applicable regulatory requirements.
  • Ability to facilitate clear communication and coordinate resources across internal (Pharma sequencing, QA, CRO, Regulatory, others) and external (IVD consultants, the drug trial sponsor).

$120,000-$165,000
The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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