Associate Director Radiobiologist- Clinical Development

Role Summary

Associate Director Radiobiologist- Clinical Development

Responsibilities

• Lead the standardization and implementation of clinical Radioligand Imaging/Therapy dosimetry protocols, ensuring consistency and scientific rigor across studies.
• Support operational excellence and provide expert dosimetry analysis within NMEH, facilitating robust and accurate trial results.
• Identify training needs and foster professional development in the team through continuous learning opportunities and mentorship initiatives.
• Set annual objectives aligned with strategic priorities and individual growth, motivating high performance and accountability among team members.
• Ensure data quality meets required standards, driving continuous improvement for reliable, high-value data across all research activities.
• Provide radiobiology leadership and encourage talent development by sharing expertise and cultivating a culture of innovation.
• Collaborate closely with global and cross-functional partners to achieve unified, organization-wide goals and share best practices.
• Drive innovation by supporting adoption of new technologies and data initiatives that advance clinical dosimetry and imaging excellence.
• Ensure compliance with GxP, regulatory standards, and participate in data governance forums to uphold data integrity and regulatory readiness.
• Manage audits, regulatory inspections, and serve as an escalation point for data quality issues, ensuring timely and effective resolution of any challenges.

Qualifications

• M.S. or PhD in physics, biology, or a clinically relevant field with a minimum of 5 years of relevant experience.
• Extensive experience with clinical dosimetry protocols in Radioligand imaging and therapy.
• Strong knowledge of radiobiology and the biological effects of ionizing radiation.
• Demonstrated expertise in positron, photon, electron, and alpha particle dosimetry, particularly for systemically administered radiopharmaceuticals.
• Proven ability to oversee data quality, regulatory compliance, and maintain GxP standards in clinical settings.
• Experience identifying training needs, mentoring teams, and fostering professional development.
• Ability to manage audits, regulatory inspections, and resolve complex data quality issues effectively.
• Strong collaboration skills, with experience working cross-functionally to implement standardized protocols and drive innovation.

Skills

• Clinical dosimetry protocols
• Radiobiology
• Dosimetry data governance
• Quality assurance and data integrity
• Cross-functional collaboration
• Regulatory compliance (GxP)

Education

• M.S. or PhD in physics, biology, or a clinically relevant field