Clinical Research Associate

This is a fully remote position, open to applicants in France.

📋 Description

• Design and evaluate clinical trials, analyze intricate medical data, and support the development of innovative treatments and therapies.

• Conduct site qualifications, initiate studies, monitor progress, and perform close-out visits.

• Ensure adherence to protocols, maintain data integrity, and prioritize patient safety throughout the duration of trials.

• Collaborate with investigators and site personnel to ensure seamless execution of studies.

• Review data and address queries to uphold the quality of clinical data.

• Assist in the preparation and review of study documentation, including protocols and clinical study reports.

• Assume responsibility for monitoring deliverables in clinical trials and work in a collaborative manner.

⛳️ Requirements

• A bachelor's degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate.

• Strong Phase I CRA experience, particularly with first-in-human (FIH) and dose escalation in early-phase oncology clinical trials.

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a keen attention to detail.

• Capability to work both independently and cooperatively in a dynamic environment.

• Willingness to travel as needed, approximately 60% of the time.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.

• Reasonable accommodations during the recruitment process.