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(Senior) Medical Science Liaison, External Research

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Illinois (USA), United States

Offer summary

Qualifications:

Advanced scientific or medical degree required, 2+ years of MSL or Medical Affairs experience, Strong knowledge in molecular oncology and biomarkers, Experience in medical writing required, Existing KOL relationships in oncology preferred.

Key responsabilities:

Support strategic account managers in research discussions
Engage with KOLs for collaborative external research
Identify data gaps and clinical needs for assays
Serve as liaison between internal teams and external investigators
Manage research portfolio tracking and medical strategy development

Tempus Unicorn https://www.tempus.com/

1001 - 5000 Employees

See more Tempus offers

Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are looking for a high-performing and experienced 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 12-15 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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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.

Additionally, for remote roles open to individuals in unincorporated Los Angeles – including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.