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Senior Medical Science Liaison, Southwest (CA, HI)

Lantheus
Full-time
Remote friendly (San Francisco, CA)
United States
$191,000 - $286,000 USD yearly
Medical Affairs

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Role Summary

The Senior Medical Science Liaison (MSL) is a key member of Global Medical Affairs, communicating scientific, 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. This is a remote position open to applicants authorized to work for any employer within the United States.

Responsibilities

  • Identifies, develops and maintains long term collaborative relationships with Key Opinion Leaders in assigned territory
  • Demonstrates strong communication skills with the ability to present approved scientific data of varying levels of complexity to internal and external customers in group and one-to-one settings, adjusted to the audience and in accordance with Company Policies and applicable laws, regulations and ethical standards
  • Responds and documents the provision of accurate, approved scientific data in response to unsolicited scientific questions or requests posed by internal and external customers for approved products/brands and for products in development
  • Shares appropriate approved clinical/technical information in a timely manner with appropriate functional teams and other internal personnel
  • Utilizes advanced clinical and technical expertise in contacts with External Experts to gain insight into diagnostic imaging patterns in prostate cancer, treatment guidelines and therapeutic advances in oncology, provider needs and patient medical needs
  • Identifies potential speakers for promotional programs and speaker training meetings
  • Provides constructive feedback to speakers regarding accuracy and delivery of approved presentations and adherence to Compliance Policies
  • Complies with Pharmacovigilance SOPs regarding Adverse Events
  • Identifies potential investigators for investigator-sponsored trials following approved processes
  • Adheres to the US โ€šร„รบCompliance Code of Conductโ€šร„รน and all applicable policies, regulations and laws

Qualifications

  • PhD, PharmD or MD required
  • 5+ years MSL experience preferred
  • 7+ years total relevant industry/clinical experience including oncology, urology, or radiopharmaceuticals/medical imaging preferred
  • Proficient at translating approved scientific or clinical data into high quality medical information for Healthcare providers
  • Demonstrated leadership in a team environment with effective communication across management, peers, and cross-functional teams
  • Highly motivated to achieve optimal results with a track record of growth and achievement
  • Ability to manage multiple tasks simultaneously and adapt to change
  • Exceptional oral and written communication skills

Other Requirements

  • Oncology and/or Radiopharmaceutical knowledge, including key scientific publications
  • In-depth knowledge of a technical, scientific or clinical area
  • Knowledge of clinical trial design and process
  • Knowledge of pharmacoeconomic data principles and implications
  • Advanced knowledge of the US Healthcare System and the Medical Imaging industry
  • Advanced Word, PowerPoint, and Excel skills
  • 70% travel required; reside near a major airport

Education

  • PhD, PharmD or MD required
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