Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

See Yourself at Telix

The Medical Science Liaison (MSL) serves as a field-based scientific and clinical expert responsible for engaging in compliant medical and scientific exchange, supporting evidence generation activities, and gathering actionable insights that inform Medical Affairs strategy. The MSL represents Telix's scientific platform and therapeutic areas of interest by developing and maintaining credible, peer-to-peer relationships with healthcare professionals and key opinion leaders.

The MSL establishes and cultivates relationships with medical experts across oncology, urology, radiology, nuclear medicine, radiation oncology, and other specialties involved in the diagnosis and management of patients within Telix's areas of focus. Through scientific exchange, the MSL communicates accurate, balanced, and clinically relevant information regarding Telix products, pipeline assets, and disease states while supporting Medical Affairs and scientific communication objectives.

In collaboration with Medical Affairs, Clinical Development, Medical Communications, and other cross-functional partners, the MSL supports clinical trial activities, evidence generation initiatives, educational programs, and insight gathering efforts. The MSL identifies and communicates emerging scientific trends, unmet medical needs, and field insights to internal stakeholders. All activities are conducted in accordance with applicable regulations, industry guidelines, and Telix policies to ensure the highest standards of scientific integrity, compliance, and patient focus.

Candidates must reside in the following areas to be considered: CA, NV, AZ, NM; relocation is not available.

Key Responsibilities

Develop and maintain peer-to-peer scientific relationships with National, Regional, and Local Key Opinion Leaders (KOLs), 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 to enhance understanding of disease states, clinical data, and Telix products and pipeline assets.
Attend scientific congresses, medical meetings, advisory boards, and investigator meetings to engage with 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 effectively with cross-functional partners, including Commercial, Clinical Operations, Medical Communications, Market Access, and Marketing, 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.