Medical Advisor - EMEA

Telix Pharmaceuticals Limited; Paris; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

Telix Pharmaceuticals Limited is seeking a Medical Advisor to support the Neuro-Oncology franchise and early access programs, collaborating with R&D, regulatory, market access and commercial teams.

You will contribute to pre-launch and launch activities, develop medical training content, engage with KOLs and advisory boards, and ensure compliance with local regulations across the EMEA region. This role emphasizes scientific leadership and cross-functional partnership.

Qualifications

• PharmD/PhD/MD or equivalent advanced scientific degree.
• At least 5 years in the pharmaceutical industry, with 2+ years in Medical Affairs.
• Strong scientific mindset and understanding of medical development, operations, and business challenges.
• Experience with product launches, KOL strategy, medical education and evidence generation.
• Experience with Early Access Programs (preferred).
• Ability to interpret scientific data, market research, and competitive intelligence.

Responsabilités

• Serve as the regional medical expert for the neuro-oncology portfolio across R&D, Clinical Operations, Regulatory Affairs, Market access and Commercial teams.
• Develop and execute the EMEA medical plan, aligning local and regional initiatives with global objectives.
• Lead the implementation and monitoring of Early Access Programs (EAPs) across the EMEA region with cross-functional collaboration.
• Conduct ongoing medical landscape monitoring, literature reviews, and critical appraisal of trial data to inform strategy.
• Develop and review medical training content for internal teams and support medical education initiatives.
• Represent the company at scientific congresses and engage with Key Opinion Leaders to capture insights.
• Support regulatory submissions and interactions with health authorities across the EMEA region.
• Contribute to publications planning, investigator meetings, and advisory boards.
• Ensure compliance with local regulations, Telix policies, and ethical standards.

Connaissances

Medical Affairs

Clinical development

KOL engagement

Regulatory knowledge

Evidence generation

Formation

Advanced scientific degree (PharmD/PhD/MD)

Description du poste

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 Advisor, will play a key role in the medical affairs department, providing medical expertise and guidance to support the development and commercialization of Telix theranostics programs with a primary focus on the Neuro-Oncology franchise and the support to Early Access Programs. This role will contribute to the pre-launch and launch activities, working closely with other departments. They will support the field medical affairs team, as well as the marketing and market access teams, providing medical input into product development and medico-marketing strategy, activity, and material. This position will support and implement the medical communication and education plans in line with the corporate and regional objectives.

Key Accountabilities

• Serve as the regional medical expert for the neuro-oncology portfolio, providing evidence-based input to support drug positioning, clinical strategy, and cross-functional decision-making across R&D, Clinical Operations, Regulatory Affairs, Market access and Commercial teams.
• Contribute to the development and execution of the EMEA regional medical plan, aligning local and regional initiatives with global strategic objectives.
• Lead the implementation, coordination, and monitoring of Early Access Programs (EAPs / Named Patient Programs / Compassionate Use Programs) across the EMEA region, in close collaboration with Regulatory Affairs, Clinical Operations, MSLs, and market access functions; ensure robust tracking of program performance, patient outcomes, and compliance with country-specific requirements.
• Conduct ongoing medical and scientific landscape monitoring, including systematic literature reviews and critical appraisal of clinical trial data, to inform, update medical strategy and support internal and external stakeholders.
• Develop and review medical training content for internal medical, sales, and marketing teams; contribute to the design and delivery of medical education initiatives for healthcare professionals (symposia, roundtables, webinars, advisory boards).
• Represent the company at scientific congresses and medical meetings; engage proactively with Key Opinion Leaders to capture, synthesize, and disseminate insights of strategic relevance.
• Participate in the design and implementation of the EMEA KOL engagement plan and medical insights collection framework, ensuring structured feedback loops inform portfolio strategy.
• Support regulatory submissions, interactions with health authorities, and clinical development activities including site selection, Phase IV studies, and registry programs.
• Actively contribute to HQ-driven Medical Affairs and clinical research activities (publication planning, investigator meetings, advisory boards).
• Ensure all medical affairs activities — including external interactions, EAP operations, and communications — are conducted in full compliance with applicable local regulations, Telix policies, and legal and ethical standards; maintain and promote up-to-date knowledge of country-specific pharmaceutical regulations across the EMEA region.

Position Requirements

• Advanced scientific, healthcare, or medical degree (PharmD, PhD, MD, RN) required.
• A minimum of 5 years of experience in the pharmaceutical industry is required, including at least 2 years in Medical Affairs, within highly scientific therapeutic areas such as Oncology or Rare Diseases.
• Strong scientific mindset with an excellent understanding of medical, clinical development/operations, and business challenges.
• A strong scientific background is mandatory.
• Thorough understanding of relevant policies guiding the Pharmaceutical Industry
• Experience supporting product launch activities, KOL strategy, medical education, and evidencegeneration initiatives
• Experience with Early Access Programs, Named Patient Programs, or Compassionate Use Programs preferred
• Experience/expertise in interpretation of scientific data, market research, and competitive intelligence tools.