Intern Gco

Johnson & Johnson

Madrid, Spain
Base: 1,000 € pm; bonus/equity: not specified; ben...
Study planning site identification
Trial documentation preparation
Study start up activities
Support the local study team in performing country and site feasibility and trial documentation

Job Summary

  • Support the local study team in performing country and site feasibility and trial documentation.
  • Assist in study start-up, execution, and close-out activities, including regulatory submissions and document management.
  • Contribute to maintaining quality standards and timelines consistent with business needs while adhering to company policies and regulations.

Matching Summary

Support the local study team in performing country and site feasibility and trial documentation.

Salary

Base: 1000 € per month; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Study Planning Site Identification
  • Trial Documentation Preparation
  • Study Start Up Activities
  • Study Execution Support
  • Study Close Out Activities
  • Adherence to ICH-GCP

Nice-to-have

  • Patient-centric approach
  • Ethical considerations
  • Proactive communication

Key Requirements

  • Degree in Pharmacy, Biology, Biotechnology, Biochemistry or similar
  • Master's degree in clinical trial monitoring
  • English B2-C1 proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter