Medical Science Liaison - West (CA, NV, AZ, NM)

Telix Pharmaceuticals (AMER)

About The Position

The Medical Science Liaison (MSL) is a field-based scientific and clinical expert who conducts compliant medical and scientific exchange, supports evidence-generation activities, and gathers actionable insights to inform Medical Affairs strategy. The MSL represents Telix's scientific platform and therapeutic areas by building and maintaining credible peer-to-peer relationships with healthcare professionals and key opinion leaders across oncology, urology, radiology, nuclear medicine, radiation oncology, and related specialties. The MSL communicates accurate, balanced, and clinically relevant information about Telix products, pipeline assets, and disease states. Working with Medical Affairs, Clinical Development, Medical Communications, and other partners, the MSL supports clinical trial activities, evidence generation, educational programs, and insight gathering. The role identifies emerging scientific trends and unmet medical needs and shares field insights with internal stakeholders, while following applicable regulations, industry guidelines, and Telix policies. Candidates must reside in California, Nevada, Arizona, or New Mexico. Relocation is not available. The territory requires extensive travel.

Requirements

Advanced healthcare or scientific degree, such as PharmD, PhD, MD, DO, DNP, NP, PA, or equivalent.
2–3 years of Medical Science Liaison experience in the pharmaceutical, biotechnology, medical device, or healthcare industry.
Demonstrated ability to build and maintain scientific relationships with healthcare professionals and key stakeholders.
Ability to communicate complex scientific and clinical information clearly and effectively to diverse audiences.
Basic understanding of Medical Affairs functions, scientific exchange, insight gathering, and evidence generation.
Experience operating in a regulated healthcare environment and adhering to compliance requirements.
Strong organizational, planning, and time-management skills, including the ability to manage multiple priorities.
Excellent verbal, written, and presentation skills.
Ability to travel extensively within the assigned territory.
Valid driver's license.
Residence in California, Nevada, Arizona, or New Mexico; relocation is not available.

Nice To Haves

Oncology experience, particularly genitourinary (GU) oncology.
Experience or interest in radiopharmaceuticals, molecular imaging, nuclear medicine, theranostics, or precision oncology.
Experience supporting clinical trials, investigator-sponsored research, or evidence-generation activities.
Familiarity with healthcare systems, treatment pathways, patient journeys, and evolving standards of care.
Experience analyzing scientific literature and communicating clinical data.
Proficiency with Microsoft Office Suite and Medical Affairs technologies.
Demonstrated ability to work effectively within cross-functional teams.

Responsibilities

Develop and maintain peer-to-peer scientific relationships with national, regional, and local key opinion leaders, investigators, and other healthcare professionals within the assigned territory.
Execute field medical activities in alignment with Medical Affairs objectives and the Medical Affairs Strategic Plan.
Gather, document, and communicate field insights, unmet needs, research opportunities, and emerging scientific trends to support Medical Affairs strategy and evidence-generation efforts.
Support clinical development activities by facilitating engagement with clinical trial sites and contributing to patient recruitment and retention initiatives, as appropriate.
Deliver accurate, balanced, and compliant scientific exchange to external stakeholders and internal partners about disease states, clinical data, and Telix products and pipeline assets.
Attend scientific congresses, medical meetings, advisory boards, and investigator meetings to engage healthcare professionals, expand scientific expertise, and communicate relevant insights to internal stakeholders.
Facilitate Medical Education Grant and Investigator-Initiated Research (IIR/IIT) processes in accordance with Telix policies and procedures.
Collaborate with Commercial, Clinical Operations, Medical Communications, Market Access, Marketing, and other cross-functional partners while maintaining appropriate compliance boundaries.
Participate in Medical Affairs initiatives, training programs, publication-related activities, advisory boards, investigator meetings, and other departmental projects.
Contribute expertise and support project work and organizational initiatives as assigned by Medical Affairs leadership.
Maintain scientific and disease-state knowledge, including awareness of competitor data, treatment landscapes, and evolving standards of care.
Maintain working knowledge of healthcare regulations, industry guidelines, and Telix policies governing healthcare professional interactions and scientific exchange.
Ensure Medical Affairs activities comply with Telix objectives, compliance policies, legal requirements, and ethical standards.
Accurately document field activities, scientific engagements, and actionable insights in approved systems and processes.
Complete required compliance, scientific, and product training.