Junior Clinical Research Associate Sponsor-dedicated
Junior Clinical Research Associate Sponsor-dedicated
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Job Description
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 IQVIAs FSP business works with the Sponsors SOPs creating more continuity for both parties.
Our models offer excellent opportunities for Junior CRAs to develop their knowledge and skills.
What we Offer:
- Excellent salary and benefits package.
- Flexible working hours in an officebased or a homebased 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 singlesponsor
- Usually allocated to 12 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 onsite 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 1 or 2 years of independent onsite 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.
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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
Required Experience:
IC
Employment Type
Full-Time
