✨ About The Role
- The Medical Director of Oncology Assay Development will provide medical guidance on new assay development and continuous assay improvement.
- They will represent medical oncology stakeholders in assay development and improvement decisions.
- The role involves assisting with regulatory and quality guidance for experimental and validation study design.
- The candidate will closely interact with clinical laboratory directors to direct assay transfer plans.
- Participation in quarterly roadmap planning for R&D resources related to assay development and improvement is expected.
âš¡ Requirements
- The ideal candidate will have an MD or DO with a current medical license, preferably in Illinois.
- They should be board certified or eligible in Molecular Genetic Pathology and have extensive experience with next-generation sequencing (NGS) assay development.
- A strong background in oncology, cancer immunotherapy, medical immunology, or clinical research is essential.
- The candidate should possess excellent organizational and communication skills, demonstrating the ability to work effectively in a fast-paced environment.
- A dynamic self-starter who can collaborate with various stakeholders, including clinical laboratory directors and R&D resources, will thrive in this role.