Experienced Clinical Research Associate - Various locations

Medpace; France; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A clinical contract research organization is seeking an Experienced Clinical Research Associate in France. In this role, you will monitor research sites, travel frequently, and communicate with medical staff. Ideal candidates will have clinical research experience and be fluent in both French and English. A bachelor's degree in a related field is required. Competitive compensation and flexible work environment are offered.

Prestations

Flexible work environment

Competitive compensation

Structured career paths

Employee health initiatives

Qualifications

• Experience as a Clinical Research Associate.
• Minimum 60-80% national travel is required.
• Outstanding communication skills.

Responsabilités

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

Connaissances

Clinical research experience

Communication skills

Detail-oriented

Time-management

Fluent in French

Fluent in English

Formation

Bachelor’s degree in a health or science related field

Outils

Microsoft Office

Description du poste

Overview

Our clinical activities are growing rapidly, and we are 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 use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Completion of monitoring reports and follow-up letters, including providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
• Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Communication with medical site staff
• Ensure good documentation practices are adhered to and communicate protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements
• Regulatory document review
• Verification and review of adverse events, serious adverse events, concomitant medications and illnesses to confirm accurate data reporting in accordance with the protocol
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement

Qualifications

• Experience as a Clinical Research Associate
• Approximately 60-80% non-local, national travel is required
• Minimum of a bachelor’s degree in a health or science related field
• Proficient knowledge of Microsoft Office
• Fluency in French & English
• Outstanding communication skills
• Detail-oriented with strong time-management

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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