Experienced Clinical Research Associate - Various locations

University Positions; Toulouse; Hybride; EUR 40 000 - 70 000; Plein temps

Résumé du poste

An established industry player is seeking an Experienced Clinical Research Associate to join their dynamic Clinical Operations team in France. This role offers an exciting opportunity to work on a variety of projects while collaborating closely with medical experts and project teams. With a focus on professional growth, you will engage in comprehensive training and have the flexibility to work from various locations in France. If you are passionate about clinical research and want to make a significant impact in the field, this position is perfect for you.

Prestations

Customized Fast PACE CRA training

Ongoing therapeutic training

Opportunities for transversal activities

Possibility to be home-based

Qualifications

• Experience as a Clinical Research Associate is essential.
• Strong communication skills and detail-oriented approach are required.

Responsabilités

• Conduct monitoring visits and ensure compliance with protocols.
• Complete monitoring reports and communicate findings effectively.

Connaissances

Clinical Research Experience

Communication Skills

Time Management

Fluency in French

Fluency in English

Detail-oriented

Formation

Bachelor’s degree in health or science-related field

Outils

Microsoft Office

Description du poste

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 possible
• Close collaboration with CRA manager
• Opportunities to work with international project teams
• 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

• Completion of monitoring reports and follow-up letters, including providing summaries of significant findings
• Conducting qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Communicating with medical site staff
• Ensuring good documentation practices and communicating protocol deviations appropriately per SOPs, GCP, and regulatory requirements
• Reviewing regulatory documents
• Verifying and reviewing adverse events, serious adverse events, concomitant medications, and illnesses to ensure accurate data reporting
• Assessing site’s patient recruitment and retention, offering suggestions for improvement
• Completing monitoring reports with summaries of significant findings, deviations, deficiencies, and recommended actions

Qualifications

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