RLT Dosimetry data flow expert

Novartis India; Hyderabad; Ibrido; INR 1.500.000 - 2.300.000; Tempo pieno

Descrizione del lavoro

Novartis India in Hyderabad seeks an RLT Dosimetry Data Flow Expert to support end-to-end dosimetry, imaging, gamma-counting, radiometabolite, and PK data delivery and review. You will work across study teams, internal functions, and external partners to ensure data quality and timely milestones.

The role requires a strong background in scientific data management, regulatory compliance, and excellent collaboration skills to harmonise data across studies and platforms.

Competenze

• Master's/PhD or pharm degree with data delivery experience.
• Experience reviewing clinical/scientific data and MED/PK datasets.
• Ability to ensure data integrity and regulatory compliance.

Mansioni

• Establish and maintain radioligand therapy dosimetry data flows.
• Review study guidance, manuals, and data-transfer specs.
• Reconcile and validate clinical, imaging, vendor, and PK datasets.
• Identify discrepancies and coordinate investigations and resolutions.
• Review final datasets and reports for study close-out.

Conoscenze

Data flow management

Clinical data review

Regulatory compliance

Data reconciliation

Communication

Formazione

Master's degree or higher

PhD

Pharmacy degree

Strumenti

EDC systems

Data management software

Descrizione del lavoro

Summary

Role Type: Hybrid Working,

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.

About The Role

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.

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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)

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)