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RLT Dosimetry data flow expert

Novartis
Hyderabad, IND
Full-time
Mid
Onsite
Discovered 1 weeks ago

Full Job Posting

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
  • Adobe Photoshop, Chemistry, Collaboration, Compensation Management, Curious Mindset, Data Pipelines, Drug Development, Employee Recruitment, Flexible Mindset, Oscilloscope, Patient Care, Sales, Small Businesses, Teamwork
  • Learn about all the ways we’ll help you thrive personally and professionally.
  • Read our handbook (PDF 30 MB)

Qualifications

  • Adobe Photoshop, Chemistry, Collaboration, Compensation Management, Curious Mindset, Data Pipelines, Drug Development, Employee Recruitment, Flexible Mindset, Oscilloscope, Patient Care, Sales, Small Businesses, Teamwork
  • 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)

Preferred Qualifications

  • Desired
  • Skills Desired

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