Experienced Clinical Research Associate, Sponsor-dedicated
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-sponsor
Usually allocated to 2-3 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
Responsible for approximately 15 sites
On site between 6 and 9 days per month, dependent on the sponsor
All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
Permanent employment contract
Sponsor 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 visits
Responsibilities:Site management and monitoring activities across France
Work with sites to adapt, drive and track subject recruitment plan
Provide protocol and study training to the assigned sites
Create and maintain monitoring visit reports and action plans
If appropriate, co-monitor, train and mentor junior members of the team Become 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 experience
Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
Have in depth GCP knowledge
Be flexible with the ability to travel nationwide
Hold a full French and clean driving license
Possess 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 development
Whatever 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.#LI-LVDW1#CRASDAJDIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at Summary
Location: Illkirch-Graffenstaden, France; Paris, France
Type: Full time