Senior Director, Clinical Diagnostics and Precision Medicine

For our client, we are seeking a Senior Director, Clinical Diagnostics and Precision Medicine to join the team of a leader in the Pharmaceuticals & Biotech space. This leader will guide a global companion diagnostics strategy that supports therapeutic pipelines and advances precision medicine initiatives. The role will translate biomarker science into actionable diagnostic plans, helping ensure the right assay strategy is aligned to clinical development, evidence generation, and regulatory expectations. You will partner closely with cross-functional teams and external diagnostic vendors to drive operational readiness, governance, and decision-making across the program lifecycle. In addition, this position will influence global CDx regulatory strategy while leading a team focused on patient selection and diagnostic execution. The work is highly collaborative and has direct impact on clinical trial enablement, assay development, and the successful progression of diagnostics from feasibility through post-approval. Location: Remote - US based candidates only, no visa sponsorship available Compensation: $242,000 – $403,300 annually Responsibilities Set and lead a global companion diagnostics strategy across therapeutic pipelines Translate biomarker biology into diagnostic target product profiles across multiple platforms Define assay selection and development strategy from feasibility through post-approval Lead a team developing diagnostic strategies for patient selection and evidence generation Oversee external IVD sponsor and partner relationships, including governance and budgets Ensure operational readiness of CDx testing in clinical trials, including workflows and data management Shape global CDx regulatory strategy in collaboration with Regulatory Affairs Qualifications Advanced degree (PhD, MD, MD/PhD, or equivalent) in a relevant scientific discipline 12+ years of experience in companion diagnostics or related fields with leadership responsibilities Proven track record leading CDx strategies through clinical development and regulatory approval Expertise in assay development and validation processes Strong understanding of global CDx regulatory pathways and obligations Experience managing external diagnostic partners and vendors Demonstrated leadership skills in mentoring and team building Benefits Remote work flexibility Opportunity to lead innovative diagnostic strategies in a cutting-edge field Collaborative environment with cross-functional teams Engagement with external partners and industry leaders Potential for professional growth and leadership development Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.