Experienced Clinical Research Associate

Medpace, Inc.; France; On-site; EUR 60,000 - 80,000; Full time

Benefits offered by this job

PACE training program

Competitive travel bonus

WFH options after training

Job summary

Medpace is seeking an Experienced Clinical Research Associate to join our Clinical/ Country Operations team in France. This role will work on a team to accomplish tasks that support the company’s success.

There is a possibility to be home based in various locations in France, with substantial travel across national and international projects. The ideal candidate has a bachelor’s degree in health or science, 60–80% non-local travel, and fluency in French and English, along with strong

Qualifications

• Bachelor’s degree in a health or science related field.
• Fluency in French & English.
• Experience as a Clinical Research Associate.
• Proficient knowledge of Microsoft Office.

Responsibilities

• Completion of monitoring reports and follow-up letters.
• Conduct qualification, initiation, monitoring, and closeout visits for sites per protocol.
• Communicate with site staff and ensure good documentation practices per SOPs, GCP and regulatory requirements.
• Review regulatory documents and adverse events data for accurate reporting.

Skills

Clinical Research Associate

French & English

Education

Bachelor's degree in health or life sciences

Tools

Microsoft Office

CTMS

Job description

Job Summary

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 use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

We offer the following:

• Customized Fast PACE® CRA training program based on your experience and therapeutic background and interest
• 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 very large pipeline of projects possibility
• Close collaboration with CRA manager
• Opportunities to work with international project team
• Competitive travel bonus
• No metric for minimum required days on site per month
• Opportunity for transversal activity like CRA lead positions, mentoring, CRA evaluator, super users, SME role.
• Possibility to be home based in various locations in France.

Responsibilities

• Completion of monitoring reports and follow-up letters.
• Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Communication with the medical site staff
• Ensure good documentation practices are being adhered to and communicating 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 corresponding 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
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications

• Experience as a Clinical Research Associate;
• Approximately 60-80% non-local, national travel is required;
• Must have a 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; and
• Must be detail-oriented and efficient in time management.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.