Tempus Labs, Inc. is hiring a
Senior Director Clinical Research in United States, Remote

Summary

The job is for a Senior Director / Vice President, Clinical Research position at Tempus, requiring a Medical Oncologist with experience in oncology clinical trials. The role involves providing medical input and oversight for assigned clinical trials and leading multidisciplinary teams. The candidate should have an MD degree, 2+ years of clinical experience as a Medical Oncologist, and 7+ years of oncology clinical trial design and execution experience.

Requirements

• MD degree
• 2+ years of clinical experience as a Medical Oncologist
• 7+ years of oncology clinical trial design and execution experience required

Responsibilities

• Serving as a Medical Director for Tempus Compass oncology clinical trials
• Leading multidisciplinary teams of trial operations and development experts to provide medical input and support
• Provide input on scientific and/or medical considerations for proposals and/or protocols
• May participate in bid defense meetings for potential projects
• Provide applicable therapeutic area training to the Tempus Compass team
• May provide therapeutic area and/or protocol training for site staff
• Provide medical oversight for assigned clinical trials including review of subject eligibility, cohort management and/or review and responding to protocol-related questions
• May attend and participate in study-specific meetings such as Site Initiation Visits, Dose Review Committee Meetings, Investigator Meetings and/or Safety Review Committee Meetings
• May perform medical review, assessment and interpretation of clinical and safety data to evaluate regulatory reporting requirements and ensure appropriate medical interpretation
• Work closely with Pharmacovigilance and Safety representatives, providing medical input into safety reports including SAE narratives and analysis of similar events, Development Safety Update Reports (DSURs) and Suspected Unexpected Serious Adverse Reaction (SUSAR) reports
• Develop study-specific Medical Monitoring Plan
• Execute or oversee execution of Medical Monitoring plan (based on study)
• Review patient lab and adverse event line listings for coding, protocol deviations, safety issues
• Attend regular internal and sponsor team meetings
• Performs other duties as assigned
• May involve travel

Preferred Qualifications

• 2+ years of experience within a CRO setting as a Medical Monitor
• Early phase oncology clinical trials experience

Benefits

• Excellent interpersonal and communication skills with ability to relate to both internal and external clients
• Thorough knowledge of ICH and local regulatory authority drug research and development regulations
• Previous experience leading teams of trial development and operations personnel
• Strong communication skills regarding the Tempus mission and strengths