Medical Director, Oncology Studies

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are looking for a Medical Director, Oncology Studies, to join the medical science team at Tempus. The ideal candidate will have experience in clinical oncology research, particularly in the areas of precision medicine.  While direct biopharma/diagnostic industry experience is preferred, it’s not required, however, in that scenario prior experience conducting clinical trials as a Principal Investigator or Co-Principal Investigator is required. 

At least 2 years of clinical research experience is required. A knowledge base in molecular diagnostics, trial development, oversight and conduct, and trial data interpretation is preferred.  Great communication and collaboration skills with both internal and external stakeholders (operations, regulatory, study site staff/physicians, etc) as well as within the study teams, is a must.  The ideal candidate will be comfortable in a dynamic environment.  This position will report directly to the VP, Oncology Studies. 

Responsibilities Include, but are not limited to:

• Serving as a medical director for Tempus Oncology Clinical Evidence and Development Trials
• Overseeing the design and conduct of all stages of studies
• Leading multidisciplinary teams of trial operations and development experts to provide medical input and support.
• Serve as medical expert for external contacts (SIVs, scientific advisory boards, academic and industry collaborations)

Required Qualifications:

• MD degree with Oncology expertise
• 2+ years of clinical research experience is required. Could be in a Clinical Research Organization, bio/pharmaceutical, or primary investigator academic research setting
• Previous experience leading teams of trial development and operations personnel
• Experience with site engagement and operations in clinical research settings
• Strong written and verbal communication skills

Preferred Qualifications: 

• Board certification or eligibility in Oncology
• Prior bio/pharmaceutical experience in Oncology Clinical Research
• Knowledge of clinical research and clinical trial design
• Familiarity with Good Clinical Practices (GCP) and regulatory interactions