Multi sponsors experienced CRA Job at IQVIA in Paris (75)
The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. As a CRA for Site Management, you will work with several sponsors on several studies following our SOPs. We seek dynamic and motivated people who truly want to make a difference in the life sciences industry. At IQVIA, we look for the very best people and give them meaningful work to do. We don’t simply think about careers, we think about contributions.
What we Offer:
Excellent salary and benefits package
Flexible working hours in an officed-based or a home-based role in Lyon or Marseille
As a CRA, you will receive a company iPad and have use of key developments such as site visit apps, visit reporting apps which allow CRAs to do their day to day job more efficiently!
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
Usually allocated to 4-5 protocols (likely to be in the areas of Oncology, Neurology, Rare diseases, ….)
Responsible for approximately 15 sites
On site between 8 and 10 days per month,
All CRAs and SCRAs are allocated a local IQVIA Line Manager
Permanent employment contract
Perform Site Selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
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 18 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 in depth GCP knowledge
Be flexible with the ability to travel nationwide
Hold a full French and clean driving licence
Possess strong communication, written and presentation skills are a must (must have fluency in English 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™.
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.
Company Location: Paris (75)