Collaborate with clinical development teams to optimize radiopharmaceutical trials, ensuring effective execution and data integrity. Contribute to study design and regulatory documents while leading components of strategic initiatives within oncology research.

Empower innovation in oncology clinical development by overseeing trial activities and collaborating cross-functionally to drive scientific integrity and regulatory compliance for life-changing radiopharmaceuticals.

Lead the charge in driving safety initiatives and benefit-risk strategies for assigned compounds. Collaborate across teams to enhance processes and ensure compliance with regulatory requirements while mentoring peers for optimum performance.

Lead the charge in safety and benefit-risk management for global programs, overseeing safety documents, signal evaluation, and cross-functional collaboration while ensuring compliance with regulatory standards and promoting quality healthcare solutions.

Advance your career by driving impactful healthcare engagements, shaping customer experiences, and collaborating across regions. Enhance product adoption by leveraging scientific expertise to meet the needs of healthcare providers and patients.