Senior Director Medical Affairs International

ABOUT CURIUM

The Group Curium is the world’s largest nuclear medicine company. At Curium, we have a singular focus – to develop, manufacture and supply world-class radiopharmaceutical products around the globe. With manufacturing facilities across Europe, Middle East and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence, and unparalleled service. As a fast-growing company in a niche market, Curium is today owned by a private equity fund with LBO financing scheme.

With over 663 M € revenues in 2024, Curium International is specialized into the production and marketing of 25+ radiopharmaceuticals products, covering 12 indications (such as oncology, cardiology, neurology pulmonary…). Our network provides optimal coverage across the world in the interest of healthcare professionals and their patients, with nearly 2,100 experienced employees and a network of 3 large manufacturing sites (Petten, Saclay and Gebze), 47 PET dedicated sites and 27 radiopharmacies.

SUMMARY OF POSITION

The Senior Director Medical Affairs International is responsible for driving the medical strategy and execution for the Theragnostic portfolio across key international markets. This role coordinates and supports country and regional field medical teams, ensuring high-quality scientific engagement, consistent medical communication, and compliant implementation of Curium medical plans.

KEY RESPONSIBILITIES

1. Drive International Medical Strategy & Evidence Generation

• Coordinate and align country medical teams and MSLs with international medical strategy, objectives, and evidence generation plans.
• Contribute to and coordinate international evidence generation activities, including company-sponsored studies, IITs/ISRs, and Real-World Evidence (RWE).
• Consolidate field medical insights to inform global strategy, life-cycle management, label expansion opportunities, and healthcare system readiness.
• Collaborate cross-functionally with Clinical Development, BioPharma, Regulatory, Market Access, Operations, and Commercial teams to support international launches, access initiatives, and implementation projects.

    2. Lead Scientific Engagement & External Medical Partnerships

• Provide strategic leadership for scientific engagement activities, including advisory boards, expert meetings, international congresses, and symposia.
• Build and maintain high-value scientific relationships with Key Opinion Leaders (KOLs), nuclear medicine specialists, radiation oncologists, and urologists across priority markets.
• Support the preparation and execution of global congress strategies, including scientific data presentations, symposia, and medical booth activities.

    3. Strengthen Medical Excellence, Field Enablement & Compliance

• Lead the development and deployment of scientific training, medical content, core slide decks, and FAQs to ensure field teams deliver accurate, balanced, and impactful scientific communication on the Theragnostic Portfolio.
• Oversee the medical review and approval of scientific and medical materials in compliance with internal SOPs and external regulations.
• Ensure all medical interactions and activities adhere to company compliance standards, local regulations, and ethical guidelines.

REQUIREMENTS

Education and Experience(s)

• Advanced degree in Life Sciences (MD, PharmD, PhD or equivalent); in a relevant life sciences discipline
• Minimum 8- 10 years of Medical Affairs experience in oncology

Required skills

• Proven experience collaborating with and/or leading MSL teams across multiple countries or regions.
• Demonstrated track record in scientific engagement, advisory boards, and congress activities in oncology.
• Solid understanding of clinical development, real-world evidence, and publication planning in an oncology setting.
• Excellent communication and presentation skills; fluent in English, additional languages an asset.
• Ability to work effectively in a matrix, multicultural environment and travel internationally as required.

Preferred skills / Soft skills

• Knowledge of the specific challenges of RLT, including diagnostic–therapeutic pairing, logistics, and health system readiness.
• Exposure to radiopharmaceuticals, radioligand therapy, or nuclear medicine
• Exposure to late-stage clinical development or regulatory processes
• Experience in both large pharma and smaller biotech environments

Salary range : 120-150 K

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. 

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. We believe diversity includes disability, and we actively encourage applications from people with disabilities. If you require any accommodations during the recruitment process, please let us know—we are happy to support you.