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Job description
Overview
Associate Director, Scientific Affairs at Tempus AI. Tempus AI expands our high-performing Scientific Affairs team to support the commercial customer focus of the Oncology Genomics business segment. We are seeking a medical affairs professional in oncology with experience in therapeutics and/or diagnostics, and with excellent communication skills to help lead the education of internal and external stakeholders on the application of Tempus NGS and additional diagnostic technologies. This position reports to the Senior Director, Medical Affairs. This remote role is open to candidates across the U.S.
Responsibilities
Function as an internal scientific/technical expert with respect to all Tempus oncology test offerings
Contribute to the development of scientifically/technically accurate and comprehensive marketing messages/collateral for external and internal stakeholders
Review and approve Oncology Marketing promotional content, outreaches, training materials, and webinars
Provide the Oncology commercial-facing teams with strategic and tactical medical support and education to incorporate Tempus oncology tissue NGS, liquid biopsy (ctDNA), and algorithmic test offerings into clinical practice
Aid in the recruitment and hiring of SALs as needed, with management of the performance and development of direct reports
Oversee day-to-day functions and management of the global medical information support team while maintaining high standards of regulatory and scientific integrity
Identify internal education gaps regarding Tempus’ oncology products and facilitate closing those gaps via multimodal approaches
Continuously update internal stakeholders on relevant medical and scientific knowledge and proactively develop market intelligence on existing competitor products and products in development
Attend key oncology clinical and scientific congresses to support coverage planning and synthesize conference learnings into internal communications
Qualifications
Fundamental understanding of molecular oncology and related clinical patient management diagnostic algorithms with NCCN, ASCO, and ESMO guidelines
Keen attention to detail in review/approval for medical/legal/regulatory content submissions
Exceptional interpersonal communication and writing skills, with strong inter- and intradepartmental management abilities and the ability to educate and train
Public speaking skills and ability to effectively communicate relevant scientific topics
Strong business acumen with ability to define strategies and manage operational plans to achieve strategic business objectives
Self-starter with an ownership mindset capable of meeting tight timelines
Working knowledge of genomic laboratory developed testing (LDT) and companion diagnostic (CDx) devices; familiarity with CLIA, CAP, Sunshine Act, and FDA-regulated diagnostic tests
Must reside in the U.S. with ability to travel (≤ 20%)
Education and Required Experience
Advanced scientific or medical degree (e.g., PhD, PharmD, MD, BSN, MSN, MS, MA, GC); doctoral degree preferred
5+ years of experience with oncology and molecular diagnostic testing in biotech or pharmaceutical industries preferred
Experience in Medical Information preferred
Salary Range: $150,000 - $180,000 USD. The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
Additionally, the Tempus Equal Opportunity statement applies. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
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.
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Worksite address
indiana, PA, 15701, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.