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Cdx Project Manager Jobs (NOW HIRING)

IQVIA

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

Experience with Companion Diagnostic (CDx) studies. * Team-oriented with excellent collaboration ... > 1 year's project management experience. * Conceptual and practical knowledge of Product ...

IQVIA, Inc.

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

Experience with Companion Diagnostic (CDx) studies. * Team-oriented with excellent collaboration ... > 1 year's project management experience. * Conceptual and practical knowledge of Product ...

IQVIA

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

Experience with Companion Diagnostic (CDx) studies. * Team-oriented with excellent collaboration ... > 1 year's project management experience. * Conceptual and practical knowledge of Product ...

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Cdx Project Manager information

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$113.7K

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How much do cdx project manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for cdx project manager in the United States is $113,676.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,500.00 and $116,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Cdx Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $113,676 per year, or $54.7 per hour.

Clinical Project Manager- IVD

Durham, NC • On-site

IQVIA
Health Care and Social Assistance • 10K+ employees
Learn more about IQVIAexternal

$93K - $232K/yr

Full-time

Re-posted 4 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

Job description

Job Summary

The Project Lead is responsible for ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements. Responsible for the timeline and budget planning and execution of studies. Assigns and ensures delivery of specific tasks to/from other members of the study team. Provides oversight to outside support including CROs, consultants and/or medical advisors.

Responsibilities

  • Leading the global study team with full accountability for study deliverables regarding quality, budget, and timelines.

  • Developing key study documents (e.g., Design Validation Plan, protocol, study training materials, study forms and templates, study report).

  • Overseeing planning and operational aspects of companion diagnostics studies sponsored by Pharma partners.

  • Ensuring adherence to regulations, guidelines, and standard operating procedures, and ensuring audit/inspection readiness.

  • Executing sponsored studies for assigned areas of focus through all study phases (planning, start-up, conduct, and close-out).

  • Overseeing projects to ensure completion on-time, within scope, and budget; tracking project performance to analyze the completion of short and long-term goals.

  • Building and maintaining strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders, and other alliance partners, including CROs.

  • Collaborating across Clinical Operations and other functions to develop and implementing best practices across Clinical Operations.

Requirements

  • Experience with Companion Diagnostic (CDx) studies.

  • Team-oriented with excellent collaboration skills with a cross-functional team.

  • Open-minded to learn new ways of doing things while leveraging previous experience.

  • Knowledge of or experience with EU In Vitro Device Regulation (IVDR) submission process

  • Minimum of a bachelor's degree in Life Science and/or relevant expertise in the Healthcare Industry or a related field, at least 5years of prior relevant experience including > 1 year's project management experience.

  • Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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