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 Benefits 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 Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

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13 Nov, 2026

Novartis

Technicien de Production - Centrale des Pesées / Support Matériel H/F

Huningue

Salary not listed

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