Clinical Research Associate 2, Sponsor-dedicated

IQVIA; Courbevoie; Hybride; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading clinical research organization in Courbevoie seeks experienced Clinical Research Associates to manage site monitoring in France, focusing on oncology, neurology, and immunology protocols. Candidates should have a degree in Life Sciences, at least 2 years of monitoring experience, and be fluently bilingual in English and French. This role offers the chance to work with cutting-edge medicines and provides genuine career development opportunities, alongside a competitive salary package.

Prestations

Excellent salary and benefits package

Flexible working hours

Career development opportunities

Qualifications

• At least 2 years of independent on-site monitoring experience.
• Experience handling multiple protocols across drug indications.
• Full French driving license required.
• Ability to travel nationwide.

Responsabilités

• Manage site monitoring activities across France.
• Adapt and track subject recruitment plans with sites.
• Provide training to assigned sites on protocol and study.
• Maintain monitoring visit reports and action plans.
• Co-monitor and mentor junior team members as needed.

Connaissances

Independent on-site monitoring experience

Time management skills

GCP knowledge

Fluent in English and French

Communication skills

Formation

Degree in Life Sciences or equivalent experience

Description du poste

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 sponsor’s 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.

What we Offer

• Excellent salary and benefits package
• Flexible working hours in an office‑based or 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 organization
• 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 in 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 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 (must have fluency in English and French)
• 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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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