Associate Director Radiobiologist overseeing clinical dosimetry protocols and providing leadership in Radioligand imaging and therapy. Supporting clinical research excellence with a focus on data quality and innovation.
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.
Requirements
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.
Benefits
Competitive salary
Flexible working hours
Professional development opportunities
Collaborative and inclusive work environment
Job title
Associate Director, Radiobiologist – Clinical Development
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