RLT Dosimetry data flow expert

Role Type: Hybrid Working, #LI-Hybrid Location: Hyderabad, India Relocation Support: Yes What if your expertise could help turn complex radioligand therapy data into reliable insights for oncology development? As an RLT Dosimetry Data Flow Expert, you will support the end-to-end delivery and review of dosimetry, imaging, gamma-counting, radiometabolite, and pharmacokinetic data. Working under guidance and across study teams, internal functions, and external partners, you will help maintain data quality, resolve issues, support key study milestones, and improve how scientific data flow across radioligand therapy and imaging studies.

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 RequirementsMaster'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 RequirementsExperience 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 NovartisHelping 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-cultureBenefits and RewardsLearn about all the ways we’ll help you thrive personally and professionally.Read our handbook (PDF 30 MB)