IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.
Leadership recognizes the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.
Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. Additionally, IQVIA’s FSP business works with the Sponsors SOP’s, creating more continuity for both parties.
Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills.
What we Offer :
- Excellent salary and benefits package
- Flexible working hours in an office-based or a home-based role in Bordeaux, Lille, Lyon, Nantes, Marseille,
- We invest in keeping our teams stable, so workload is consistent
- We offer genuine career development opportunities for those who want to grow as part of the organisation
- We give the chance to work on cutting edge medicines, right at the forefront of new medicine development
Role Details :
Working in partnership with a single-sponsorUsually allocated to 2-3 protocols (likely to be in the areas of Oncology, Neurology, Immunology and / or Diabetes)Responsible for approximately 15 sitesOn site between 6 and 9 days per month, dependent on the sponsorAll CRAs and SCRAs are allocated a dedicated IQVIA Line ManagerPermanent employment contractSponsor model has reduced travel (approx. 30% or less) due to using ‘the Risk-Based monitoring which incorporates remote monitoring therefore there is less need for on-site visitsResponsibilities :
Site management and monitoring activities across FranceWork with sites to adapt, drive and track subject recruitment planProvide protocol and study training to the assigned sitesCreate and maintain monitoring visit reports and action plansIf appropriate, co-monitor, train and mentor junior members of the teamBecome part of our team.
We believe in hiring the best talent in the industry.
To become part of our team, you should :
Have a degree in Life Sciences or have equivalent experience within a nursing background.Have at least 2 years of independent on-site monitoring experienceBe experienced in handling multiple protocols across a variety of drug indications with good time management skillsHave in depth GCP knowledgeBe flexible with the ability to travel nationwideHold a full French and clean driving licensePossess strong communication, written and presentation skills are a must (must have fluency in English and French language)With the merger between Quintiles and IMS Health, we now have access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. It’s the next generation of clinical developmentWhatever your career goals, we are here to ensure you get there!We invite you to join IQVIA™.
Join Us
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at