
Medical Science Liaison, Oncology
Posted Jul 25

Posted Jul 25
This is a fully remote position, open to applicants in California, +1 more state.
β’ Act as the field-based scientific authority for the oncology portfolio, facilitating the implementation of Medical Affairs strategies and regional medical plans.
β’ Create and implement a territory engagement strategy that identifies and prioritizes key opinion leaders (KOLs), investigators, academic institutions, community oncology practices, and other relevant external stakeholders within the designated area.
β’ Conduct balanced, non-promotional, and scientifically accurate exchanges of medical information regarding disease states, treatment landscapes, clinical evidence, product details, treatment guidelines, and unmet medical needs.
β’ Address unsolicited medical and scientific inquiries in line with Cosette Medical Affairs policies and coordinate follow-ups with Medical Information or other relevant internal partners as necessary.
β’ Capture, document, and relay actionable field-based scientific insights concerning treatment patterns, evidence gaps, competitive landscapes, emerging oncology trends, and stakeholder needs.
β’ Assist in research initiatives, including facilitating investigator-initiated trials, identifying and supporting Cosette-sponsored study sites, and coordinating interactions with investigators or advisory groups alongside Clinical Development and Medical Affairs.
β’ Provide support for medical congress coverage, advisory board meetings, scientific communications, medical education initiatives, speaker training, and review of scientific content as needed.
β’ Collaborate cross-functionally with teams in Medical Affairs, Medical Information, Clinical Development, Market Access, Commercial, Regulatory, Legal, and Compliance, while upholding the non-promotional function of Medical Affairs.
β’ Maintain comprehensive and current expertise in assigned disease areas, Cosette products, market dynamics, clinical trial data, treatment guidelines, and the regulatory/compliance framework governing field medical operations.
β’ Ensure timely and thorough documentation of stakeholder engagements, insights, follow-up activities, training, expenses, and other necessary records.
β’ Operate in full compliance with Cosette policies, the PhRMA Code, OIG guidance, FDA regulations, and applicable federal and state laws, including requirements for reporting adverse events and product complaints.
β’ A minimum of 2 years of experience in oncology MSL or a similar field medical role is required.
β’ Experience in engaging with oncology KOLs, academic institutions, community oncology practices, clinical investigators, or multidisciplinary cancer care teams within the assigned territory.
β’ Strong comprehension of oncology disease states, treatment landscapes, clinical trial design, evidence interpretation, treatment guidelines, and compliant scientific communication.
β’ Proven ability to engage with external experts and convey complex scientific information clearly, accurately, credibly, and in compliance with regulations.
β’ A terminal scientific or clinical degree is required (PharmD, PhD, MD, or DO).
β’ Competitive salary and performance-based bonuses.
β’ Comprehensive health benefits including medical, dental, and vision coverage.
β’ Opportunities for professional development and continuing education.
β’ Flexible working arrangements to promote work-life balance.
β’ Retirement savings plan with company matching contributions.
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