Experienced Clinical Research Associate, Sponsor-dedicated
$31,200–$31,200 year
On-siteCourbevoie, Île-de-France, France
Job Summary
Manage site monitoring activities across approximately 15 sites in France, adapting and tracking subject recruitment plans while providing protocol and study training. Create and maintain monitoring visit reports and action plans, utilizing risk-based monitoring to reduce travel needs. Collaborate with a single sponsor on 2-3 protocols in Oncology, Neurology, Immunology, or Diabetes, co-monitoring and mentoring junior team members as appropriate. Work 6 to 9 days per month on-site with a dedicated line manager. Join IQVIA's FSP business to contribute to specific sponsor pipelines and access next-generation data pools for efficient site selection.
Required Qualifications
- Degree in Life Sciences or equivalent experience within a nursing background
- At least 2 years of independent on-site monitoring experience
- Experience in handling multiple protocols across a variety of drug indications
- Good time management skills
- In depth GCP knowledge
- Ability to travel nationwide
- Full French and clean driving license
- Fluency in English and French language
- Strong communication, written and presentation skills
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