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Avantages offerts par ce poste
Competitive salaries and benefits
Departmental study/training
Mentoring opportunities
Internal growth opportunities
Employee referral program
Employee recognition programs
Loyalty Award Program
Résumé du poste
A leading biopharmaceutical company in Paris is seeking a Clinical Research Associate II / Senior Clinical Research Associate to monitor clinical trials and ensure compliance with regulations. The role requires at least 2 years of independent monitoring experience, strong communication skills in English and French, and the ability to manage site relationships. Competitive salary and benefits are offered, with opportunities for professional development.
Qualifications
Minimum of 2 years as an independent site monitor in clinical trials, ideally in oncology or rare disease.
Strong understanding of ICH-GCP and regulatory guidelines.
Comfortable working independently and managing priorities.
Responsabilités
Independently manage all aspects of monitoring for assigned clinical trials.
Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
Build strong site relationships and ensure high-quality data collection.
Identify and resolve site issues, escalating as needed.
Mentor and support junior CRAs.
Connaissances
Leading monitoring activities
Site relationship management
Problem-solving
Clear communication in English and French
Description du poste
A leading biopharmaceutical company in Paris is seeking a Clinical Research Associate II / Senior Clinical Research Associate to monitor clinical trials and ensure compliance with regulations. The role requires at least 2 years of independent monitoring experience, strong communication skills in English and French, and the ability to manage site relationships. Competitive salary and benefits are offered, with opportunities for professional development.
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