Medical Director, Tempus Studies

Employment Type: Full-time

Salary: $275,000 - $310,000 (This range is applicable if the role is performed from Illinois and may vary for other locations such as California, Colorado, New York. Actual salary may vary based on qualifications and experience.)

Location Type: [Not Specified]

Position Overview

Passionate about precision medicine and advancing the healthcare industry? Tempus is seeking a Medical Director, Tempus Studies, to join our medical science team. This role is crucial for overseeing high-priority observational and interventional studies within the Tempus AI Studies group. As the primary clinical expert, you will be responsible for study design, protocol development, and study execution, collaborating with multidisciplinary teams and representing Tempus externally to biopharma collaborators and clinical researchers. You will also provide critical medical input to advance various Tempus AI initiatives by collaborating with other business units within the organization.

Responsibilities

• Serve as a medical director for select programs to advance the business initiatives of Tempus Studies.
• Oversee and lead the design and conduct of all stages of select studies.
• Provide and source expert medical opinions to guide study design and protocol development across a variety of indications and treatment paradigms.
• Lead multidisciplinary teams of trial operations and development experts to execute key study partnerships in line with appropriate timelines and milestones, providing medical and regulatory expertise as needed.
• Represent Tempus Studies externally to launch studies and lead Site Initiation Visits (SIVs), scientific advisory boards, steering committees, and other academic and industry collaborations.

Requirements

• MD degree with Oncology expertise OR MD with oncology clinical research experience.
• 2+ years of clinical trials experience (in a clinical research organization, biotech/biopharma company, or as a primary investigator in an academic research setting).
• Previous experience leading teams of trial development and operations personnel.
• Experience with clinical trial data review & medical monitoring, site engagement, and clinical trial operations.
• Strong written and verbal communication skills.
• Familiarity with Good Clinical Practices (GCP) and regulatory interactions.

Company Information

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.

Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Application Instructions

[Not Specified]