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Junior Clinical Research Associate, Sponsor-dedicated

Aplica ya
Mapa de ubicación: Courbevoie, France Full time R1280048

Descripción del trabajo

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 Junior CRA’s to develop their knowledge and skills.

What we Offer:

  • Excellent salary and benefits package.
  • Flexible working hours in an office-based or a home-based role.
  • 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 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
  • Responsible for approximately 10 sites
  • On site between 6 and 8 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

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.
  • Have at least 6 months of independent on-site monitoring experience
  • Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
  • Have a GCP knowledge
  • Be flexible with the ability to travel nationwide
  • Hold a full French and clean driving license
  • Possess good communication, written and presentation skills are a must (must have fluency in English and French language)
  • 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.

Forge a career with greater purpose, make an impact, and never stop learning.

#LI-LVDW1

#CRASDAJD

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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