Job Description
Summary Support oncology in the delivery of high-quality dosimetry data from radioligand therapy or radioligand imaging studies. The 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.

Job Description

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. Essential Requirements
• 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 Requirements
• 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. Why Novartis Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Perks and Rewards Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Skills Desired Chemistry, Clinical Pharmacology, Clinical Research, Drug Discovery Process, Medical Research, Patient Care, Physiology, Quality Control (QC), Research and Development, Simulation Software, Taking Initiative, Translational Medicine

📌 RLT Dosimetry Data flow Expert (Hyderabad)
🏢 Novartis
📍 Hyderabad