Oncology Clinical Scientist Intern (Hybrid)

Johnson & Johnson Co.; Geel; Hybride; EUR 16 000 - 21 000; Plein temps

Résumé du poste

Johnson & Johnson Belgium is offering an Oncology Clinical Scientist Intern position designed for undergraduates and graduates to contribute to oncology research and clinical trials. You will work within a global clinical team, supported by mentors, on a 12-week program with hybrid on-site and remote elements.

The role provides hands-on experience in trial protocols, data interpretation, literature review, and collaboration across disciplines, with emphasis on regulatory documentation and poster

Qualifications

• Must be currently enrolled in an accredited university or college program throughout the duration of the internship.
• Must not be graduating before, during, or after the start of the internship.
• Fluent in written and spoken English.
• Self-motivated and a future scientist leader with strong organizational skills.

Responsabilités

• Assist with management of trial activities including patient screening and eligibility reviews.
• Assist with document processing and management within the electronic master file (vTMF).
• Participate in department and team meetings and cross-functional team activities.
• Develop study training materials and documents for the internship projects.
• Shadow key clinical roles to gain practical exposure and learn regulatory expectations.
• Support trial start-up activities and data review processes as needed.

Connaissances

Leadership

Communication

English

Formation

Enrollment in university program

GPA 3.0 or higher

Outils

Excel

OneNote

Outlook

PowerPoint

SharePoint

Teams

Word

Slack

Description du poste

Johnson & Johnson Belgium is offering an Oncology Clinical Scientist Intern position designed for undergraduates and graduates to contribute to oncology research and clinical trials. You will work within a global clinical team, supported by mentors, on a 12-week program with hybrid on-site and remote elements.

The role provides hands-on experience in trial protocols, data interpretation, literature review, and collaboration across disciplines, with emphasis on regulatory documentation and poster