Associate Director, MSL Central Region
$150,000–$250,000 year
On-siteTexas, United States or Iowa, United States
Job Summary
Tempus is seeking an Associate Director, MSL Central Region to lead and mentor a team of Medical Science Liaisons, develop and execute strategic plans for disseminating scientific information, and engage with key opinion leaders, healthcare professionals, and other stakeholders to support clinical and scientific objectives. The role involves coordinating with cross-functional teams (clinical development, marketing, sales) on product launches, monitoring industry trends, ensuring regulatory compliance in the dissemination of scientific information, and representing Tempus at conferences. Candidates should have an advanced scientific degree, substantial MSL and leadership experience, strong oncology and molecular biology knowledge, and proven relationship-building and strategic planning abilities. Travel up to 50% and remote work from multiple US states are supported; preferred candidates have experience in precision medicine, data analytics, and prior people management.
Required Qualifications
- Advanced degree (PhD, PharmD, MD, DO, or DNP) in a relevant scientific discipline (e.g., oncology, molecular biology, genetics)
- Minimum of 5 years of experience in a Medical Science Liaison or other relevant medical role, and/or at least 2 years in a relevant managerial or leadership position in industry is strongly preferred
- Strong knowledge of oncology, molecular biology, and the healthcare landscape
- Solid tumor oncology therapeutic knowledge or expertise
- Excellent communication, presentation, and interpersonal skills
- Proven ability to build and maintain relationships with KOLs and other stakeholders
- Strong strategic thinking and problem-solving skills
- Ability to travel (up to 50%)
- Working knowledge of genomic laboratory-developed testing (LDT) and familiarity with CLIA-88’, CAP guidelines; Working knowledge of IVD regulatory guidelines from the FDA (21 CFR Part 809, CFR Part 820, 21 CFR Part 807, 21 CFR Part 812, 21 CFR Part 814) and Sunshine Act (2013)
Desired Qualifications
- Prior people management experience is strongly preferred
- Experience in precision medicine or personalized healthcare (preferred)
- Familiarity with data analytics and artificial intelligence in healthcare (preferred)
- Travel up to 50% (required by role)
- Strong strategic thinking and problem-solving skills
- Excellent communication, presentation, and interpersonal skills
- Solid tumor oncology therapeutic knowledge or expertise
- Working knowledge of genomic LDT, CLIA/CAP, and FDA IVD regulatory guidelines (FDA 21 CFR parts) (preferred)
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