Distinguished Scientist, Companion Diagnostics

MSD•Rahway, NJ

3d•Hybrid

About The Position

The Distinguished Scientist/ Executive Director within Companion Diagnostics (CDx) Development, will lead one of our company's Diagnostic Development Teams (DxDTs), supervising PhD-/MD-level employees, developing and overseeing CDx strategy development, alignment and execution for specific projects, including associated digital pathology (DP) projects when applicable. Position reports to Associate Vice President, Companion Diagnostics (CDx).

Requirements

PhD Required
Minimum of 8 years of experience in industry setting
Extensive experience with one or more major biomarker platforms (i.e. NGS, IHC, PCR)
Knowledge of the discovery, development and application of biomarkers in support of decision making for drug development and as CDx
Demonstrated track record in the development and approval of CDx
Demonstrated expertise in diagnostic development as evident by peer review publication record, patents, and/or products
Demonstrated experience in developing and implementing strategic approaches across functional groups and in conjunction with global pharma teams
Demonstrated experience in working with clinical teams to support design, implementation and analysis of clinical trials incorporating key biomarkers in order to yield data that can support CDx development and regulatory submissions
Familiarity with requirements for EU IVDR, China HGRAC, Japan PMDA, and other global markets for CDx development/registration
Proven decision-making and planning skills
High level of verbal and written communication skills including presentation capabilities to senior executives
Analytical Thinking
Assay
Bioanalytical Techniques
Biomarker Development
Clinical Trials
Communication
Companion Diagnostics (CDx)
Drug Development
Innovation
Leadership
Scientific Leadership
Strategic Foresight

Nice To Haves

Experience in both pharma and Dx settings
Deep technical knowledge in an area of focus such as circulating tumor DNA (ctDNA), immunohistochemistry/ pathology, digital pathology, etc.
Experience directly interfacing in meetings and written documents with global health authorities
Current Employees apply HERE
Current Contingent Workers apply HERE
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Responsibilities

Lead cross-functional DxDT including Regulatory, Commercial, Business Development, Project Management, Operations, Clinical Development, Statistics, Bioinformatics, etc. to drive CDx strategy, development and implementation of CDx projects – and associated DP when relevant – for a portfolio of various assets/biomarkers, mainly in the therapeutic area of Oncology
Supervise PhD-/MD-level employees leading and executing diagnostic projects within CDx subteams and coordinating the work conducted with our external Dx partners, including associated DP efforts when needed
Partner with internal stakeholders (e.g. clinical/asset teams, Biomarker Leads, CDx Regulatory, Commercial) to assess DxDT needs and develop strategies to address those needs
Contribute to the selection of appropriate assays, platforms and Dx partners for the execution of biomarker strategies, including overseeing possible design/execution of pilot studies with Dx vendors
Identify and assess novel technologies/platforms with potential for CDx application
Oversee team preparation of Dx-related regulatory documents including, for example, pre-submissions, briefing books, IDEs, IVDR PSAs, PMAs, and participation in meetings with global regulatory agencies to provide CDx expertise
Oversee team members performing operational tasks required to execute assigned projects as needed, e.g. ordering samples, QC of incoming clinical trial biomarker results, assay/data transfer troubleshooting, etc.
Serve as a subject matter expert within our company, collaborating with project teams, biomarkers, clinical operations, regulatory affairs, medical affairs and commercial on the implementation of global CDx assay strategies in global clinical trials
Oversee internal project-level senior management and governance interactions relevant to CDx
Oversee DxDT input into preclinical and early-stage oncology programs
Provide CDx expertise/assessment for due diligence teams