RLT Dosimetry Data flow Expert

About the Role

Support oncology in the delivery of high-quality dosimetry data from radioligand therapy or radioligand imaging studies. This role facilitates reliable end-to-end flow of dosimetry, imaging, gamma-counting, radio metabolite, and PK-related data, supports timely data review and issue resolution, and provides structured coordination across internal functions, study teams, and external partners. Activities are performed under guidance appropriate to the Principal Scientist I or II level.

Key Responsibilities

• Establish and maintain radioligand therapy dosimetry data flows in line with agreed roles and responsibilities.
• Review electronic case report forms, study guidance, manuals, and data-transfer specifications supporting scientific assessments.
• Reconcile and validate clinical, laboratory, imaging, vendor, gamma-counting, and pharmacokinetic datasets.
• Identify data discrepancies and coordinate timely investigation, escalation, troubleshooting, and resolution.
• Review final datasets, vendor dosimetry reports, and pharmacokinetic and dosimetry outputs for study reporting.
• Coordinate assigned final analyses and close-out activities for radioligand therapy and imaging studies.
• Support platform harmonisation, process optimisation, training, and implementation of lessons learned.
• Ensure activities meet applicable procedures, quality standards, data-integrity expectations, and safety requirements.

Requirements & Tech Stack

• Master's degree, Doctor of Philosophy, Doctor of Pharmacy, or equivalent qualification in a relevant scientific or quantitative discipline.
• Academic, internship, laboratory, clinical-research, or industry experience relevant to scientific data delivery and review.
• Understanding of clinical or scientific data flows involving imaging, laboratory, vendor, or pharmacokinetic data.
• Ability to review, reconcile, and validate complex datasets with accuracy and attention to detail.
• Ability to identify data discrepancies and support timely investigation, escalation, and resolution.
• Strong organisational and coordination skills, with the ability to support multiple study activities and milestones.
• Effective communication and collaboration skills for working across internal functions, study teams, and external partners.
• Understanding of regulated working practices, quality requirements, data integrity, and procedural compliance.

Desirable

• Experience or strong interest in radioligand therapy, dosimetry, nuclear medicine imaging, or related quantitative work.
• Experience in a pharmaceutical, biotechnology, contract research, healthcare, academic, or similarly regulated environment.
• Familiarity with electronic case report forms, data-transfer specifications, data cleaning, vendor oversight, or scientific reporting.
• Knowledge of gamma-counting, radiometabolite analysis, pharmacokinetics, imaging data, or clinical study close-out activities.