Clinical Research Associate (associate Site Manager)

Johnson & Johnson

Issy-les-Moulineaux, France
**
Gcp, sops, local laws, and regulations
Site initiation and start-up
Site monitoring and close-out
** Johnson & Johnson is seeking a Clinical Research Associate (Associate Site Manager) for their Global Clinical Operations Team in Issy-les-Moulineaux, France. This entry-level role involves managing clinical trial sites, ensuring compliance with protocols and regulations, and facilitating communication between the sponsor and investigational sites. **

Job Summary

  • An Associate, Site Manager is an entry level site management role with typically 0-2 years of experience, serving as the primary contact point between the Sponsor and the Investigational Site.
  • Responsibilities include assisting with site selection, qualification, initiation, monitoring, and close-out activities, ensuring compliance with protocols, SOPs, GCP, and applicable regulations.
  • The role requires proficiency in French and English, strong IT skills, and a willingness to travel, partnering with the Local Trial Manager and central study team to ensure overall site management.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Clinical Research Associate (Associate Site Manager) for their Global Clinical Operations Team in Issy-les-Moulineaux, France. This entry-level role involves managing clinical trial sites, ensuring compliance with protocols and regulations, and facilitating communication between the sponsor and investigational sites. **

Skills & Requirements

Must-have

  • GCP, SOPs, local laws, and regulations
  • site initiation and start-up
  • site monitoring and close-out
  • adverse event reporting
  • essential document management

Nice-to-have

  • process improvement and training
  • therapeutic area experience
  • risk-based monitoring model implementation
  • investigator meeting participation

Key Requirements

  • BA or BS degree in Pharmacy, Nursing, Life Sciences, or related scientific field
  • 1 year of clinical trial monitoring experience
  • Proficient in speaking and writing French and English

Work Rights

Not specified

Tailored Resume

Cover Letter