Key responsibilities:

• Support the mapping and structuring of Central Radiopharmacies in Canada and US, including vendor qualification and contract negotiation support. 
• Support the contracting of specialized vendors and provide legal coordination for technical agreements and contracts.
• Act as a regional point of contact for nuclear medicine infrastructure, including equipment, suppliers, and radiolabeling processes.
• Collaborate with local and global stakeholders to ensure the technical and operational feasibility of RLT studies.
• Identify gaps and propose solutions to enhance the country’s readiness and capacity for conducting radiopharmaceutical studies.
•  Assist studies in securing RLT supplies, supporting with vendor process excellence during Study Start-Up (SSU) and throughout trial conduct.
•  Partner with SSU, Clinical Operations, Legal, Quality, Procurement and Regulatory Affairs teams, without assuming direct responsibilities from these areas.
• Contribute to the development of regional playbooks, procedures and best practices for RLT studies.
• Oversight of selection, qualification, & management of Radiopharmacy (both central and site) activities
• Oversight of management of nuclear medicine equipment related tasks (i.e. Dose Calibrator calibrations, Gamma Counter calibrations, SPECT/CT qualifications, PET/CT qualifications, procurement of equipment)

Essential Requirements:

• Bachelor’s degree in Pharmacy, Biomedicine, Biomedical Engineering, Medical Physics, or related fields.
• Solid knowledge of radiopharmacy and nuclear medicine, including cold kit radiolabeling processes and operation of equipment such as gamma cameras, PET/CT, and hot cells.
• Familiarity with local and international regulations applicable to radiopharmaceuticals and basic knowledge of compliance and quality standards relevant to clinical studies involving radioactive products.
• Experience in mapping and qualifying technical and logistical vendors for radiopharmaceutical studies.
• Understanding of importation, transportation, and storage processes for radioactive materials.
• Ability to read and interpret technical documents, including product dossiers, safety data sheets, clinical protocols, and technical contracts.
• Strong stakeholder management skills with technical profiles, including clinical engineers, medical physicists, pharmacists, and nuclear medicine specialists.
• Fluent in English and French

Desirable Requirements: (

•  Previous experience in clinical research, preferably with exposure to projects involving radiopharmaceuticals or nuclear medicine.
• •Strategic mindset and ability to navigate complex and ambiguous environments.

At Novartis Canada, we are determined to be a valued partner and advocate, with a deep understanding of patient needs along the entire care journey – from drug development, to diagnosis, to access and beyond. Part of the way we are doing this is by leveraging data, technology, and partnerships.

Research & Development: we focus on four core therapeutic areas: Cardiovascular, Renal & Metabolic, Immunology, Neuroscience and Oncology. We also develop and deliver treatments through other promoted and established brands, which today are helping millions of patients. Over the last three years, our average annual research and development investment in Canada was over $30 million, and we conduct clinical trial research in every region throughout Canada.

Commitment to Diversity and Inclusion: Novartis is committed to building outstanding, inclusive work environment and diverse team’s representatives of the patients and communities we serve.