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Experienced Clinical Research Associate
il y a 1 mois
As a Clinical Research Associate, you will be working in partnership with a single sponsor, allocated to 2-3 protocols, and responsible for approximately 15 sites. You will be on site between 6 and 9 days per month, dependent on the sponsor. This role offers excellent opportunities for experienced CRAs to expand their knowledge and skills.
Key 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
Requirements
- 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)
About Us
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 https://www.iqvia.com/
