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 the team's expertise aligns with the company's objectives.
• Ensure all pharmacology and toxicology studies adhere to regulatory guidelines, including FDA, EMA, and other relevant agencies.
• Prepare and review relevant sections of regulatory submissions.
• Collaborate cross-functionally with other departments such as research, clinical development, regulatory affairs, and quality assurance to ensure seamless product development.
• Analyze and interpret pharmacological and toxicological data to guide decision-making processes and provide insights into the safety and efficacy of radiopharmaceutical products.
• Conduct thorough risk assessments to identify potential safety concerns and develop strategies to mitigate risks associated with radiopharmaceutical products.
• Implement best practices and innovative approaches to enhance the company's product development efforts.
• Manage the departmental budget effectively, ensuring optimal allocation of resources and cost-effective execution of projects.
• Effectively communicate pharmacology and toxicology findings, recommendations, and updates to senior management, regulatory agencies, and external stakeholders as required.
• Function independently when interacting with global health authorities.

Education And Experience

• PhD or equivalent degree in Pharmacology, Toxicology, or a related scientific field required.
• A DVM or PharmD with relevant experience may also be considered.
• 10+ years of experience in pharmacology and toxicology, preferably within the radiopharmaceutical or pharmaceutical industry.
• Strong knowledge of regulatory guidelines and requirements related to pharmacology and toxicology studies, particularly in the context of radiopharmaceuticals.
• Excellent analytical, problem-solving, and decision-making skills.
• Effective communication skills, with the ability to present complex scientific information clearly and concisely to diverse audiences.
• Demonstrated ability to work collaboratively in a cross-functional environment.

Key Capabilities

• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected.
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges.
• Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do.
• Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results.
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders.
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges.
• Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language.
• Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals.
• Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges.
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills.

About the role

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.

Qualifications

• PhD or equivalent degree in Pharmacology, Toxicology, or a related scientific field required.
• A DVM or PharmD with relevant experience may also be considered.
• 10+ years of experience in pharmacology and toxicology, preferably within the radiopharmaceutical or pharmaceutical industry.
• Strong knowledge of regulatory guidelines and requirements related to pharmacology and toxicology studies, particularly in the context of radiopharmaceuticals.
• Excellent analytical, problem-solving, and decision-making skills.
• Effective communication skills, with the ability to present complex scientific information clearly and concisely to diverse audiences.
• Demonstrated ability to work collaboratively in a cross-functional environment.

Skills

• Strong knowledge of regulatory guidelines and requirements related to pharmacology and toxicology studies, particularly in the context of radiopharmaceuticals.
• Excellent analytical, problem-solving, and decision-making skills.
• Effective communication skills, with the ability to present complex scientific information clearly and concisely to diverse audiences.
• Demonstrated ability to work collaboratively in a cross-functional environment.

Benefits

• Competitive salaries.
• Annual performance-based bonuses.
• An equity-based incentive program.
• Generous vacation.
• Paid wellness days.
• Support for learning and development.

Pay

N/A

Schedule

N/A