Clinical Research Associate 2, Sponsor-dedicated

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

Résumé du poste

A leading clinical research organization is seeking a Clinical Research Associate (CRA) to manage and monitor clinical sites across France, particularly in oncology, neurology, immunology, and diabetes. The CRA will have a permanent contract and is expected to work closely with sites to enhance subject recruitment and provide training. Candidates must have at least 2 years of independent on-site monitoring experience and hold a degree in Life Sciences or equivalent, along with fluency in English and French. This role offers a flexible working environment and a chance for career growth.

Prestations

Excellent salary and benefits package

Flexible working hours

Career development opportunities

Qualifications

• At least 2 years of independent on-site monitoring experience.
• Experience in handling multiple protocols across various drug indications.
• Clean driving license required for travel nationwide.

Responsabilités

• Manage and monitor clinical sites across France.
• Drive and track subject recruitment plans.
• Train sites on protocol and study requirements.
• Create monitoring visit reports and action plans.
• Mentor junior team members as needed.

Connaissances

Independent on-site monitoring

Time management

Strong communication skills

GCP knowledge

Fluency in English

Fluency in French

Formation

Degree in Life Sciences or equivalent experience

Description du poste

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.

We invite you to join IQVIA™.

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!

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.