Clinical Research Associate

TFS HealthScience; United States; Remote; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Clinical Research Associate to join their dedicated team. This role involves supporting ongoing clinical studies, ensuring high-quality data collection, and compliance with regulatory standards. The ideal candidate will have prior experience in clinical research, particularly in medical devices and cardiovascular studies. You will be part of a collaborative environment that values innovation and aims to make a positive impact on patients' lives. If you possess strong communication skills and a proactive attitude, this opportunity offers personal and professional growth in a rewarding setting.

Benefits

Competitive compensation package

Comprehensive benefits

Opportunities for personal growth

Collaborative work environment

Qualifications

• 1-3 years of CRA experience, preferably in medical devices.
• Strong communication and organizational skills required.

Responsibilities

• Conduct regular monitoring visits and review study data.
• Maintain communication with study sites for progress and issues.

Skills

Clinical Research Experience

Communication Skills

Organizational Skills

Problem-Solving

Fluency in French

Working Knowledge of English

Job description

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.