Associate Director, Scientific Affairs, Indiana

OverviewAssociate 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.ResponsibilitiesFunction as an internal scientific/technical expert with respect to all Tempus oncology test offeringsContribute to the development of scientifically/technically accurate and comprehensive marketing messages/collateral for external and internal stakeholdersReview and approve Oncology Marketing promotional content, outreaches, training materials, and webinarsProvide 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 practiceAid in the recruitment and hiring of SALs as needed, with management of the performance and development of direct reportsOversee day-to-day functions and management of the global medical information support team while maintaining high standards of regulatory and scientific integrityIdentify internal education gaps regarding Tempus' oncology products and facilitate closing those gaps via multimodal approachesContinuously update internal stakeholders on relevant medical and scientific knowledge and proactively develop market intelligence on existing competitor products and products in developmentAttend key oncology clinical and scientific congresses to support coverage planning and synthesize conference learnings into internal communicationsQualificationsFundamental understanding of molecular oncology and related clinical patient management diagnostic algorithms with NCCN, ASCO, and ESMO guidelinesKeen attention to detail in review/approval for medical/legal/regulatory content submissionsExceptional interpersonal communication and writing skills, with strong inter- and intradepartmental management abilities and the ability to educate and trainPublic speaking skills and ability to effectively communicate relevant scientific topicsStrong business acumen with ability to define strategies and manage operational plans to achieve strategic business objectivesSelf-starter with an ownership mindset capable of meeting tight timelinesWorking knowledge of genomic laboratory developed testing (LDT) and companion diagnostic (CDx) devices; familiarity with CLIA, CAP, Sunshine Act, and FDA-regulated diagnostic testsMust reside in the U.S. with ability to travel (= 20%)Education and Required ExperienceAdvanced scientific or medical degree (e.g., PhD, PharmD, MD, BSN, MSN, MS, MA, GC); doctoral degree preferred5+ years of experience with oncology and molecular diagnostic testing in biotech or pharmaceutical industries preferredExperience in Medical Information preferredSalary 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.J-*****-Ljbffr