Global Oncology Clinical Research Scientist – TTFields

Novocure Inc; Portsmouth (NH); Hybrid; USD 125,000 - 185,000; Full time

Benefits offered by this job

Annual bonus

RSU grant

Benefits package

Job summary

Novocure Inc. is seeking a Clinical Research Scientist to advance global oncology clinical development programs evaluating TTFields. You will lead scientific direction, engage investigators and clinical sites, and shape study design from concept through completion.

You will build partnerships across Clinical Development, Medical Affairs, Data Management, and Regulatory Affairs while delivering robust clinical insights and ensuring GCP compliance in a fast-paced environment.

Qualifications

• Strong understanding of clinical research methodology and study design.
• Experience supporting clinical data review and interpretation.
• Excellent communication and interpersonal skills for cross-functional collaboration.

Responsibilities

• Contribute to planning, design, execution, analysis, and interpretation of global oncology clinical development programs.
• Translate strategies into high-quality studies meeting scientific/regulatory objectives.
• Author and coordinate study protocols, amendments, reports, and publications.
• Partner with Clinical Operations and Data Management to support study execution and data quality.
• Lead medical data review activities and identify emerging insights.
• Prepare materials for investigator meetings, DMCs, steering committees, and leadership presentations.
• Foster relationships with investigators and clinical researchers throughout studies.

Skills

Clinical research

Oncology experience

Data interpretation

Communication

Travel 40%+

Education

MD/PhD/ PharmD

Job description

Novocure Inc. is seeking a Clinical Research Scientist to advance global oncology clinical development programs evaluating TTFields. You will lead scientific direction, engage investigators and clinical sites, and shape study design from concept through completion.

You will build partnerships across Clinical Development, Medical Affairs, Data Management, and Regulatory Affairs while delivering robust clinical insights and ensuring GCP compliance in a fast-paced environment.