Director, Clinical Science
$192,600–$240,800 year
Remote · California, United States or US
Job Summary
Director, Clinical Science to architect trial strategies and protocol execution for an oncology molecular diagnostics portfolio, focusing on signal studies and pipeline expansion; lead cross-functional collaboration across clinical development, biostatistics, and translational data science to design, validate, and execute robust clinical protocols, informed consent documents, and data reviews while ensuring regulatory compliance and data integrity; mentor junior staff and drive cross-site trial delivery within a remote US context.
Required Qualifications
- Advanced degree in Life Sciences (MD, PhD, PharmD, MS, RN, or equivalent) required
- 10+ years of clinical development experience within the pharmaceutical/biotechnology/diagnostic industry, with a direct focus on oncology trials
- Deep understanding of oncology molecular diagnostics, companion diagnostics (CDx), liquid biopsy performance metrics, or MRD validation pipelines preferred
- Proven track record driving clinical data review workflows, trial data cleaning cycles, protocol development, and technical data reporting
- Sound foundational knowledge of FDA regulations, global health authority trial standards, and Good Clinical Practice (GCP) guidelines
- Experience directly managing scientific personnel and building cross-functional trial delivery structures
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