Clinical Research Associate

TFS HealthScience; Paris; Sur place; EUR 40 000 - 70 000; Plein temps

Résumé du poste

An established industry player is seeking a Clinical Research Associate to join their dedicated SRS team. This role involves supporting clinical studies for a global medical device company focused on cardiovascular therapies. You will play a crucial role in ensuring high-quality data collection and compliance while maintaining communication with study sites. The position offers a competitive compensation package and opportunities for personal and professional growth in a collaborative and innovative environment. If you're passionate about making a difference in patients' lives, this is the perfect opportunity for you.

Prestations

Competitive Compensation Package

Comprehensive Benefits

Opportunities for Personal Growth

Opportunities for Professional Growth

Qualifications

• 1-3 years experience as a CRA, ideally in medical devices and cardiovascular studies.
• Fluency in French and good English communication skills required.

Responsabilités

• Conduct regular monitoring visits and ensure compliance with regulatory requirements.
• Maintain communication with study sites and address their needs.

Connaissances

Communication Skills

Interpersonal Skills

Organizational Skills

Attention to Detail

Solution-oriented Mindset

Fluency in French

Working Knowledge of English

Formation

Bachelor's Degree in Life Sciences

Description du poste

About this role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions.

We are currently looking for a Clinical Research Associate (CRA) to join our SRS team, dedicated to one sponsor, a global medical device company with a strong focus on cardiovascular therapies.

The CRA will support ongoing clinical studies in (North) France. You will play a key role in ensuring high quality data collection and compliance.

Key Responsibilities

1. Perform regular monitoring visits and co-monitoring visits
2. Review study data and ensure it meets regulatory and sponsor requirements
3. Maintain communication with study sites to ensure study progress and address any site needs or issues
4. Ensure all site documentation is complete and up to date
5. Collaborate closely with the staff to support workload and maintain study quality

Qualifications

1. Prior experience as a CRA, preferably one to three years, ideally within medical devices and cardiovascular studies
2. Excellent communication and interpersonal skills, with a dynamic, proactive and collaborative attitude
3. Strong organizational skills with attention to detail and a solution-oriented mindset
4. Willing to travel to sites across Northern France as needed
5. Fluency in French and a good working knowledge of English

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You will be joining a team that values collaboration, innovation, and making a difference in the lives of patients.