Fellow, Nonclinical Sciences

Key Accountabilities
- Provide strategic direction and oversight for pharmacology and toxicology activities related to radiopharmaceutical development.
- Design, plan, and oversee preclinical pharmacology and toxicology studies to support regulatory submissions and product development.
- Lead, mentor, and develop a team of scientists and researchers focused on pharmacology and toxicology.
- Ensure studies adhere to regulatory guidelines (e.g., FDA, EMA) and prepare/review relevant sections of regulatory submissions.
- Collaborate cross-functionally with research, clinical development, regulatory affairs, and quality assurance.
- Analyze and interpret pharmacological and toxicological data to guide safety/efficacy decisions.
- Conduct risk assessments and develop mitigation strategies for radiopharmaceutical safety concerns.
- Stay current on advances in pharmacology, toxicology, and radiopharmaceutical research; implement best practices.
- Manage departmental budget and allocate resources cost-effectively.
- Communicate findings and recommendations to senior management, regulators, and external stakeholders as needed.
- Independently interact with global health authorities.

Education and Experience / Requirements
- PhD (or equivalent) in Pharmacology, Toxicology, or related scientific field (DVM or PharmD with relevant experience may be considered).
- 10+ years’ experience in pharmacology and toxicology (preferably radiopharmaceutical/pharmaceutical industry).
- Strong knowledge of regulatory guidelines for pharmacology/toxicology studies (radiopharmaceutical context).
- Excellent analytical, problem-solving, and decision-making skills.
- Strong communication skills; can present complex scientific information clearly.
- Proven ability to work cross-functionally.