×
Register Here to Apply for Jobs or Post Jobs. X

Director, Companion Diagnostic Program Manager

Remote / Online - Candidates ideally in
Princeton, Mercer County, New Jersey, 08543, USA
Listing for: Genmab
Remote/Work from Home position
Listed on 2026-07-08
Job specializations:
  • Management
    Regulatory Compliance Specialist, Project & Program Management
Salary/Wage Range or Industry Benchmark: 194560 - 291840 USD Yearly USD 194560.00 291840.00 YEAR
Job Description & How to Apply Below

The Role & Department

As a Director, Companion Diagnostic Program Manager, you will be part of the Program Management function and will be responsible for providing strategic and operational leadership for the planning, development, validation, and execution of companion diagnostic assays (CDx) projects across our oncology portfolio.

The role leads CDx sub‑teams, in partnership with CDx SMEs to ensure that the CDx strategy (where applicable) is effectively integrated into the Compound Development Plan and Target Product Profile. This position is responsible for delivering compliant, high‑quality diagnostic solutions aligned with clinical development timelines and regulatory expectations.

You will report to the Head of Program Management and work closely with colleagues from Translational & Quantitative Sciences (including the Companion Diagnostic expert team), Clinical Strategy, Regulatory, Commercial, Market Access and external diagnostic collaborators.

Key Responsibilities
  • Lead development of CDx strategy for oncology programs from early through late‑stage development and global Health Authority approvals in partnership with CDx SMEs, who will represent the CDx sub team on Compound Development Team.
  • Providing strategic guidance and driving cross‑functional alignment for programs requiring predictive biomarkers.
  • Provide strategic and operational leadership for the development and execution of integrated CDx plans supporting patient selection, therapeutic assessment, regulatory approval, and commercial viability of CDx assays, in partnership with CDx SMEs.
  • Ensure CDx timelines and deliverables are aligned with clinical development milestones, regulatory submissions, and commercialization plans.
  • Present CDx strategy, progress and results to senior leadership, governance committees, and external stakeholders in collaboration with CDx SMEs.
  • Lead preparation of presentations to governance committee to support decision‑making related to diagnostic strategy, execution, and vendor selection.
  • Oversee external diagnostic partnerships in collaboration with Alliance Management, including scope definition, performance oversight, risk management, issue resolution, budget accountability, and working with Joint Steering Committee members.
  • Partner with CDTL/PM of the compound, Clinical Strategy, Precision Medicine, Regulatory Affairs, and Quality functions to ensure alignment with protocol, regulatory, and operational requirements.
  • Support inspection readiness and participate in internal and external audits, including regulatory inspections and partner audits.
Requirements
  • Bachelor’s degree in Biological Sciences, Bioengineering or a related field, with a minimum of 10 years of experience in diagnostics, pharmaceuticals, or the life sciences industry.
  • Seven or more years of experience in project management, portfolio strategy or related leadership roles.
  • Experience in oncology and immuno‑oncology drug development, with demonstrated success in driving biomarker‑based patient selection strategies in hematologic malignancies and/or solid tumors.
  • Working knowledge of CDx development processes including analytical and clinical validation strategies, design controls, and global regulatory interactions related to CDx submissions.
  • Demonstrated ability to lead cross‑functional teams and effectively manage external vendors and strategic partners.
  • Demonstrated experience managing complex program budgets and external vendor contracts, with accountability for forecasting, financial planning, and resource allocation.
  • Advanced proficiency with Microsoft Project and/or enterprise planning platforms such as Planisware.
  • US‑based candidates are required. This position offers flexible work arrangement, including remote work or a hybrid presence from our Princeton, NJ or Boston, MA offices.

For US based candidates, the proposed salary band for this position is $—$. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long‑term incentives.

Benefits

When you…

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary