Clincal Data Lead

Overview

Join to apply for the Clincal Data Lead role at Novocure .

At Novocure, we are transforming cancer care with Tumor Treating Fields (TTFields) – an innovative, non-invasive therapy for aggressive tumors like glioblastoma. With 25 years of pioneering science behind us, we remain driven by bold thinking and a clear mission: together with our patients, we strive to extend survival in some of the most challenging cancers.

We are seeking a Clinical Data Lead (f/m/d) to join our Global Clinical Operations team in Switzerland.

In this pivotal role, you will oversee outsourced data management activities, ensure inspection-ready clinical trial data, and support successful regulatory submissions.

Key responsibilities:

• Lead sponsor data management deliverables from study start-up to database lock
• Oversee CRO and vendor activities, ensuring high-quality, compliant data
• Maintain oversight of third-party data sources (labs, imaging, ePRO)
• Align data review strategies with the Clinical Study Team (CST)
• Review and approve study-specific Data Quality Documentation (DQD)

Your profile:

• Bachelor’s in Life Sciences, Health Informatics, Computer Science, or related field
• 5+ years of clinical data management experience, incl. 2–3 years in a lead role
• Proficiency with EDC systems and knowledge of CDISC standards, GCP, and regulatory requirements
• Strong communication and collaboration skills across cross-functional teams

As part of our NovoFlex hybrid policy, this role requires in-office presence in Baar, Switzerland at least three times per week.

If you’re motivated to advance oncology innovation and ensure the highest quality of clinical trial data, we’d love to hear from you.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Project Management and Analyst

Industries

• Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research

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