Senior Medical Science Liaison, External Research

🕒 June 26

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Logo of Tempus AI

Tempus AI

1001 - 5000 employees

Founded 2015

🏥 Healthcare

🧬 Biotechnology

🤖 Artificial Intelligence

Healthcare • Biotechnology • Artificial Intelligence

Tempus AI is an advanced healthcare technology company that specializes in precision medicine through the use of AI and genomic profiling. The company provides innovative solutions across various medical fields, including oncology, cardiology, neurology, and psychiatry. Tempus enables healthcare providers to make informed treatment decisions by integrating real-world data, clinical trial matching, and algorithmic testing to improve patient outcomes and accelerate drug development.

📋 Description

• Provide medical support to strategic account managers to ensure successful management of research discussions and intake of study concepts for potential collaborations • Engage academic KOLs and investigators in oncology to work on collaborative external research with Tempus • Proactively seek opportunities for incorporating Tempus assays into high-impact external research • Identify data gaps and clinical unmet needs in key cancer types for each Tempus assay platform or molecular signature • Assess study proposals received from investigators for completeness, clarity, feasibility, clinical and scientific merit, and strategic value • Serve as research liaison between internal data scientists and external academic investigators for all study-related communications • Support medical writing of abstracts, data presentations, and manuscripts on external research study collaborations • Collaborate with the Medical Affairs Team and other internal teams in supporting medical advisory boards

🎯 Requirements

• 2+ years of Medical Science Liaison or other Medical Affairs experience in the diagnostics, biotech, or pharmaceutical industries • Existing KOL relationships in the field of oncology is preferred • Strong public speaking skills • Working knowledge of statistical methods and clinical trial design principles is preferred • Working knowledge of genomic laboratory-developed testing (LDT); familiarity with CLIA-88’, CAP, Sunshine Act (2013) • Advanced scientific or medical degree (PhD, PharmD, MD, MSN, BSN) • Advanced knowledge and experience in molecular oncology, biomarkers, and diagnostic platforms in clinical oncology is required • Experience in medical writing for abstracts, scientific presentations, and manuscripts is required • Formal education and experience in conducting translational or clinical research in oncology is strongly desired • Experience working in clinical settings, particularly within academic institutions, is strongly desired.

🏖️ Benefits

• Incentive compensation • Restricted stock units • Medical and other benefits

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