Associate Director Radiobiologist- Clinical Development

Healthcare Businesswomen’s Association; City Of London; On-site; GBP 50,000 - 75,000; Full time

Job summary

A leading healthcare organization seeks a Radiobiologist to oversee clinical dosimetry protocols and ensure high standards within the Nuclear Medicine Expert Hub. You will lead operational excellence, oversee data quality, and drive continuous improvement in a collaborative environment. Ideal candidates have an advanced degree and extensive experience in clinical dosimetry, with a strong understanding of radiobiology. You'll have the opportunity to influence global drug development while working with world-class scientists.

Qualifications

• Minimum of 5 years of relevant experience in clinical dosimetry.
• Strong knowledge of radiobiology and ionizing radiation effects.
• Proven ability to ensure data quality and regulatory compliance.

Responsibilities

• Lead standardization and implementation of dosimetry protocols.
• Support operational excellence within Nuclear Medicine Expert Hub.
• Manage audits and regulatory inspections effectively.

Skills

Clinical Research

Data Analysis

Budget Management

Risk Management

Coaching

Cross-Functional Teams

Clinical Trial Protocol

Risk Monitoring

Education

M.S. or Ph.D. in physics, biology, or a clinically relevant field

Job description

Job Description Summary

Location: London, United Kingdom; Dublin, Ireland; Barcelona, Spain

As a Radiobiologist, you will play a key role within the Nuclear Medicine Expert Hub (NMEH), working closely with clinical colleagues to develop, implement, and uphold standards for clinical dosimetry protocols in radioligand imaging and therapy.

You oversee quality assurance across all protocols involving radioligand imaging, ensuring high standards for imaging and dosimetry with a focus on the biological effects of ionizing radiation, providing expert guidance and operational input, leveraging deep knowledge of positron, photon, electron, and alpha particle dosimetry, especially for systemically administered radiopharmaceuticals.

You will also be overseeing clinical dosimetry data, reinforcing adherence to standard processes, data quality, and supporting the governance of these procedures.

As a subject matter expert, you identify and resolve clinical data quality issues, drive continuous improvement, and ensure timely escalation of unresolved concerns to maintain the integrity of clinical research activities.

This is a unique opportunity to influence global drug development while working alongside world‑class scientists in a highly supportive, matrixed environment.

Your Key Responsibilities

• Lead the standardization and implementation of clinical radioligand imaging/therapy dosimetry protocols, ensuring consistency and scientific rigor across studies.
• Support operational excellence and provide expert dosimetry analysis within NMEH, facilitating robust and accurate trial results.
• Identify training needs and foster professional development in the team through continuous learning opportunities and mentorship initiatives.
• Set annual objectives aligned with strategic priorities and individual growth, motivating high performance and accountability among team members.
• Ensure data quality meets required standards, driving continuous improvement for reliable, high-value data across all research activities.
• Provide radiobiology leadership and encourage talent development by sharing expertise and cultivating a culture of innovation.
• Collaborate closely with global and cross‑functional partners to achieve unified, organization‑wide goals and share best practices.
• Drive innovation by supporting adoption of new technologies and data initiatives that advance clinical dosimetry and imaging excellence.
• Ensure compliance with GxP, regulatory standards, and participate in data governance forums to uphold data integrity and regulatory readiness.
• Manage audits, regulatory inspections, and serve as an escalation point for data quality issues, ensuring timely and effective resolution of any challenges.

Essential Requirements

• M.S. or Ph.D. in physics, biology, or a clinically relevant field with a minimum of 5 years of relevant experience.
• Extensive experience with clinical dosimetry protocols in radioligand imaging and therapy.
• Strong knowledge of radiobiology and the biological effects of ionizing radiation.
• Demonstrated expertise in positron, photon, electron, and alpha particle dosimetry, particularly for systemically administered radiopharmaceuticals.
• Proven ability to oversee data quality, regulatory compliance, and maintain GxP standards in clinical settings.
• Experience identifying training needs, mentoring teams, and fostering professional development.
• Ability to manage audits, regulatory inspections, and resolve complex data quality issues effectively.
• Strong collaboration skills, with experience working cross‑functionally to implement standardized protocols and drive innovation.

Why Novartis?

We believe new insights, perspectives, and ground‑breaking solutions can be found at the intersection of medical science and digital innovation. We are committed to building an inclusive, diverse workplace that reflects the communities we serve. Join us and help reimagine medicine for millions of patients worldwide.

Commitment to Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Join our Novartis Network

If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Skills Desired

Budget Management, Clinical Research, Clinical Trial Protocol, Clinical Trials, Coaching, Cross‑Functional Teams, Data Analysis, Learning Design, Lifesciences, Risk Management, Risk Monitoring