Clinical Research Associate 2

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 department, you may work across different therapeutic areas following our internal 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
- in addition to classic technology (laptop and smartphone), 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 organization
- We give the chance to work on cutting edge medicines, right at the forefront of new medicine development
- Office-based or home-based role

**Role Details**:

- Usually allocated to 4-5 protocols (likely to be in the areas of Oncology, Neurology, Inflammatory diseases, Rare diseases, gastroenterology, pediatrics.)
- Responsible for approximately 15 sites
- All CRAs are allocated a local IQVIA Line Manager
- Permanent employment contract

**Responsibilities**:

- Perform Site Selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice
- 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 12 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 license

Possess strong communication, written and presentation skills are a must (must have fluency in French and 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.