FULL-TIME
Posted Jul 31, 2026
Job Description
Description: At Novocure, every role contributes to extending the lives of people living with cancer. As our new Clinical Research Scientist, you'll play a key role in advancing our global clinical development programs and bringing innovative therapies closer to patients.
Reporting to the Senior Clinical Research Scientist within Global Clinical Development, this is an opportunity to shape the scientific direction and execution of innovative oncology clinical trials evaluating Tumor Treating Fields (TTFields). This role offers a unique blend of scientific leadership and direct engagement with investigators and clinical sites. Beyond contributing to protocol development, clinical strategy, and data interpretation, you'll build meaningful partnerships with investigators, participate in study-related site activities, and help ensure the successful execution of clinical trials from concept through completion.
Working at the intersection of science and operations, you'll collaborate with cross-functional teams across Clinical Development, Clinical Operations, Medical Affairs, Data Management, Regulatory Affairs, Safety, and Device Support Specialists. If you're energized by combining scientific expertise with real-world clinical engagement and want to make a tangible impact on patients' lives, this role offers an exceptional opportunity to do just that.
WHAT YOU'LL DO
As a key scientific member of our Global Clinical Development team, you will:
• Contribute to the planning, design, execution, analysis, and interpretation of global clinical development programs across multiple oncology indications.
• Translate clinical development strategies into high-quality studies that meet scientific, regulatory, and business objectives.
• Author, review, and coordinate key clinical documents, including study protocols, protocol amendments, clinical study reports, ClinicalTrials.gov summar
Reporting to the Senior Clinical Research Scientist within Global Clinical Development, this is an opportunity to shape the scientific direction and execution of innovative oncology clinical trials evaluating Tumor Treating Fields (TTFields). This role offers a unique blend of scientific leadership and direct engagement with investigators and clinical sites. Beyond contributing to protocol development, clinical strategy, and data interpretation, you'll build meaningful partnerships with investigators, participate in study-related site activities, and help ensure the successful execution of clinical trials from concept through completion.
Working at the intersection of science and operations, you'll collaborate with cross-functional teams across Clinical Development, Clinical Operations, Medical Affairs, Data Management, Regulatory Affairs, Safety, and Device Support Specialists. If you're energized by combining scientific expertise with real-world clinical engagement and want to make a tangible impact on patients' lives, this role offers an exceptional opportunity to do just that.
WHAT YOU'LL DO
As a key scientific member of our Global Clinical Development team, you will:
• Contribute to the planning, design, execution, analysis, and interpretation of global clinical development programs across multiple oncology indications.
• Translate clinical development strategies into high-quality studies that meet scientific, regulatory, and business objectives.
• Author, review, and coordinate key clinical documents, including study protocols, protocol amendments, clinical study reports, ClinicalTrials.gov summar
Additional Details
- State
- New Hampshire
- Country
- US
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