Experienced Clinical Research Associate, Sponsor-dedicated

2 LOCATIONS (OTHER)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

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-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.

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#CRASDAJD

IQVIA 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 https://jobs.iqvia.com

REQUIRED VERIFIED SKILLS

GCP
Clinical Research
Excel
SOP

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Experienced Clinical Research Associate, Sponsor-dedicated position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Career path typically progresses from Associate, to Senior Specialist, and eventually to Manager or Lead positions within the department.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: GCP, Clinical Research, Excel. Prepare real-world examples demonstrating these skills for the interview.
RECOMMENDED TRAINING
1/5

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