Experienced Clinical Research Associate Sponsor-dedicated

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 startup 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 SOPs, creating more continuity for both parties.

Our models offer excellent opportunities for experienced CRAs 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
• Genuine career development opportunities for those who want to grow as part of the organisation
• Opportunity to work on cutting-edge medicines, at the forefront of new medicine development
• 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
• Sponsor model has reduced travel (approx. 30% or less) due to using ‘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 the 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

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 (must have fluency in English and French)

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.