Senior Clinical Research Associate
HybridParis, Île-de-France, France
Job Summary
Independently monitor Phase II–IV clinical trials in France across multiple therapeutic areas including Oncology to ensure compliance with ICH-GCP and regulatory requirements. Conduct site qualification, initiation, monitoring, and close-out visits while managing study documentation, regulatory submissions, and ethics/IRB approvals. Resolve issues and provide support to ensure successful trial execution, ensuring high-quality data and patient safety. Collaborate with cross-functional teams and site staff to facilitate smooth trial operations, provide training to site staff, and maintain effective relationships with stakeholders. Requires residency in Paris or Lyon with a hybrid or remote schedule.
Required Qualifications
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements within a CRO environment
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Fluency in French
- Professional proficiency in English
- Strong organizational and communication skills
- Attention to detail
- Residency in the Paris or Lyon areas
- Legal right to work in the country where the role is based
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