We are looking for a high-performing and experienced Medical Science Liaison (MSL) / Senior Medical Science Liaison (Sr. MSL) to support the commercial, research, and educational objectives of the company. We are seeking a field-based MSL with a strong clinical and scientific background in oncology, genomic testing, and excellent communication skills to educate healthcare providers about Tempus assays and technologies. We are considering candidates residing either in Chicago or in a field-based location within the US.
Responsibilities- Provide medical support to strategic account managers (Precision Medicine Program 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, including investigator-initiated trials, assay grants for biobank samples or prospective trials, and real-world retrospective data studies
- Proactively seek opportunities for incorporating Tempus assays into high-impact external research, including collaborations with cooperative group trials and pharmaceutical trials (company-sponsored or investigator-led trials)
- 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, including iterative workflows in reviewing analyses and study results
- Support medical writing of abstracts, data presentations, and manuscripts on external research study collaborations
- Support engagements with potential research collaborators through regularly scheduled specialty-specific Tempus+ Working Group meetings, which include faculty from a broad range of academic and community oncology centers
- Manage and leverage KOL relationships gained through study collaborations to support broader research and educational interests for the organization
- Collaborate with the Medical Affairs Team and other internal teams in supporting medical advisory boards
- Contribute to team tracking and management of the External Research Portfolio, including abstract and Publication Planning/execution efforts
- Support the development and management of a Medical Research Strategy and Scientific Exchange Plans to guide the prioritization of new external research investments through conducting biannual clinical reviews of unmet needs for biomarkers for immunotherapy and targeted therapies, tumor response monitoring, and minimal residual disease in each cancer type
- Liaison cross-functionally with internal stakeholders in Medical Affairs, Marketing, Sales, R&D, Clinical Development, Biostatistics, Bioinformatics, and Al engineers
- Attend oncology conferences and cooperative group research meetings with the objectives of connecting with KOLs and providing comprehensive meeting synopses and summaries of high-impact scientific content
- Continuously update internal stakeholders on relevant medical and scientific knowledge as well as proactively sharing market intelligence
Required Skills- 2+ years of Medical Science Liaison or other Medical Affairs experience in the diagnostics, biotech, or pharmaceutical industries is required
- Ability to project manage up to 25-30 individual study collaborations in different phases of execution is essential
- Ability to work with commercial field-based sales and business account managers is essential.
- Ability to communicate, liaison, and manage expectations effectively with KOLs and academic researchers is essential
- Existing KOL relationships in the field of oncology is preferred.
- Strong public speaking skills and ability to effectively communicate relevant scientific topics and concepts internally to cross-functional teams and externally to physicians and researchers
- 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)
- Self-starter with an ownership mindset able to work and deliver on tight timelines
- Ability to travel (up to 50%)
Educational and Experience Requirements- 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
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$120,000-$190,000
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.
