Senior Medical Science Liaison, Southwest; CA,
San Francisco, San Francisco County, California, 94199, USA
Listed on 2026-02-01
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Healthcare
Medical Imaging
About Lantheus
Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years.
Today, we're expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.
At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We're dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.
Join us and be part of a company where your contributions make a real impact, because we know someone's health is in our hands.
Job SummaryThe Sr. MSL is a key member of Global Medical Affairs, communicating scientic, clinical and technical information within the medical community, developing and maintaining strong collaborative relationships with Key Opinion Leaders and serving as a therapeutic and radiopharmaceutical expert with internal audiences. Preferred candidates will reside near an international airport.
The Sr. MSL demonstrates expertise and extensive knowledge in the eld of oncology, radiopharmaceuticals, medical imaging trends, clinical trials and scientic activities within the oncology therapeutic and medical imaging arena. Continuously updates this expertise and knowledge based on training direction and approved resources provided.
This is a remote position open to applicants authorized to work for any employer within the United States.
Responsibilities and essential functions:- Identies, develops and maintains long term collaborative relationships with Key Opinion Leaders in assigned territory
- Demonstrates strong communication skills with the ability to present approved scientic data of varying levels of complexity to internal and external customers in both group and one-to-one settings, appropriately adjusted to the audience and in accordance with Company Policies, and applicable laws, regulations and ethical standards
- Demonstrates appropriate response and documents the provision of accurate, approved scientic data in response to unsolicited scientic questions or requests posed by internal and external customers for approved Products/Brands and for products in development in accordance with Company Policies, and applicable laws, regulations and ethical standards
- Shares appropriate approved clinical/technical information in a timely manner with the appropriate functional teams and other internal personnel.
- Utilizes advanced clinical and technical expertise in contacts with External Experts, in accordance with the strategy developed by the Company and Compliance Policies to further understand and gain insight into (1) diagnostic medical imaging patterns in prostate cancer (2) treatment guidelines and therapeutic advances in the oncology arena, (3) the needs and interests of Healthcare providers, and (4) the medical needs of patients
- Identies potential speakers for promotional programs and speaker training meetings
- Provides constructive feedback to speakers and Lantheus (e.g., Professional Promotions) regarding accuracy and delivery of approved presentations and adherence to Compliance Policies
- Fully understands and complies with Lantheus Pharmacovigilance SOPs regarding Adverse Events
- Identies potential investigators for investigator sponsored trials following approved processes
- Adheres to the US "Compliance Code of Conduct" and all LMI policies and procedures, the OIG Guidance, the PhRMA Code, GCP, HIPAA and relevant FDA laws and regulations (certify completion where required)
- PhD, Pharm
D or MD required - 5+ years MSL experience preferred
- 7+ years total relevant industry/clinical experience including oncology, urology, or…
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