Experienced Clinical Research Associate - Various locations

Medpace; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

A leading company in clinical research is seeking an Experienced Clinical Research Associate to join their team. This role involves monitoring clinical trials, ensuring compliance with protocols, and collaborating with medical staff. The position offers opportunities for travel and professional growth, with options for home-based work in France.

Benefits

Customized fast PACE CRA training program

User-friendly CTMS

Ongoing therapeutic training

Competitive travel bonus

Opportunities for transversal activities

Qualifications

• Experience as a Clinical Research Associate required.
• 60-80% non-local, national travel required.

Responsibilities

• Complete monitoring reports and follow-up letters.
• Conduct qualification, initiation, monitoring, and closeout visits.
• Communicate with medical site staff.

Skills

Communication

Detail-oriented

Time Management

Fluent in French

Fluent in English

Education

Bachelor’s degree in health or science-related field

Tools

Microsoft Office

Job description

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical/Country Operations team in France. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you can use your previous expertise and develop further, this is the opportunity for you.

We offer the following:

• Customized fast PACE CRA training program based on your experience and therapeutic background
• User-friendly CTMS with electronic submission and approval of monitoring visit reports
• Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
• National assignments with a large pipeline of projects
• Close collaboration with CRA manager
• Opportunities to work with an international project team
• Competitive travel bonus
• No metric for minimum required days on site per month
• Opportunities for transversal activities like CRA lead positions, mentoring, CRA evaluator, super users, SME roles
• Possibility to be home-based in various locations in France

Responsibilities

• Complete monitoring reports and follow-up letters, including summaries of significant findings
• Conduct qualification, initiation, monitoring, and closeout visits in compliance with protocols
• Communicate with medical site staff
• Ensure good documentation practices; communicate protocol deviations per SOPs, GCP, and regulations
• Review regulatory documents
• Verify and review adverse events, serious adverse events, medications, and illnesses for accurate data reporting
• Assess patient recruitment and retention at research sites, providing suggestions for improvement
• Summarize significant findings, deviations, deficiencies, and recommended actions for compliance

Qualifications

• Experience as a Clinical Research Associate
• Approximately 60-80% non-local, national travel required
• Bachelor’s degree in health or science-related field
• Proficient in Microsoft Office
• Fluent in French & English
• Excellent communication skills
• Detail-oriented and efficient in time management