Clinical Research Associate

il y a 1 mois


Paris, Île-de-France IQVIA Temps plein

At IQVIA, we're dedicated to delivering quality results for our clients. As a Clinical Research Associate - Sponsor Dedicated, you'll play a key role in our FSP business, working closely with a single sponsor partner to drive success.

Our FSP model is unique in the industry, with teams dedicated to a single sponsor partner. This allows us to build strong relationships and deliver tailored solutions that meet our clients' needs. As a Clinical Research Associate, you'll be responsible for site management and monitoring activities across France, working with sites to adapt, drive and track subject recruitment plans.

We're looking for a talented individual with a degree in Life Sciences or equivalent experience, and at least 6 months of independent on-site monitoring experience. You'll need to be experienced in handling multiple protocols across a variety of drug indications, with good time management skills and a GCP knowledge. Fluency in English and French is a must, and you'll need to hold a full French and clean driving license.

We offer a competitive salary and benefits package, flexible working hours, and genuine career development opportunities. You'll have the chance to work on cutting-edge medicines, right at the forefront of new medicine development. If you're passionate about delivering quality results and making a positive impact on human health, we'd love to hear from you.

Key Responsibilities:

  • Site management and monitoring activities across France
  • Work with sites to adapt, drive and track subject recruitment plans
  • Provide protocol and study training to assigned sites
  • Create and maintain monitoring visit reports and action plans

What We Offer:

  • Competitive salary and benefits package
  • Flexible working hours
  • Genuine career development opportunities
  • Chance to work on cutting-edge medicines

Requirements:

  • Degree in Life Sciences or equivalent experience
  • At least 6 months of independent on-site monitoring experience
  • Experienced in handling multiple protocols across a variety of drug indications
  • Good time management skills and GCP knowledge
  • Fluency in English and French
  • Full French and clean driving license


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