Hybrid Clinical Research Associate 2 – Sponsor-dedicated

Posted last month

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About the role

  • Clinical Research Associate managing site activities across multiple protocols for a single sponsor. Engaging in monitoring, training, and recruitment efforts for clinical studies.

Responsibilities

  • Manage site activities and monitoring across France
  • Collaborate with sites to develop, drive and track subject recruitment plans
  • Deliver protocol and study training to assigned sites
  • Create and maintain monitoring visit reports and action plans
  • Where appropriate, co-monitor, train and mentor junior team members

Requirements

  • Degree in Life Sciences or equivalent nursing experience
  • Minimum 2 years of independent on-site monitoring experience
  • Experience managing multiple protocols across various drug indications with strong time-management skills
  • In-depth knowledge of GCP
  • Flexible and able to travel nationwide
  • Hold a full, clean French driving license
  • Strong verbal, written and presentation skills; fluency in English and French required

Benefits

  • Competitive salary and benefits package
  • Flexible working hours with office-based or home-based options
  • Professional development opportunities
  • Opportunity to work on cutting-edge medicines

Job title

Clinical Research Associate 2 – Sponsor-dedicated

Job type

Experience level

JuniorMid level

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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