Clinical Research Associate France

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

Résumé du poste

An established industry player is seeking a Clinical Research Associate to join their team in Strasbourg. This role offers the chance to work in a dynamic environment, managing investigator sites and ensuring compliance with ICH-GCP guidelines. With a focus on career growth and internal training, you will play a vital role in the drug development process, collaborating with a global team to make a significant impact in healthcare. If you are passionate about clinical research and eager to contribute to life-saving projects, this opportunity is perfect for you.

Prestations

Annual Bonuses

Comprehensive Health Benefits

Retirement Plans

Flexible Work Environment

Qualifications

• Experience in managing investigator sites in clinical research.
• Knowledge of ICH-GCP and regulatory requirements.

Responsabilités

• Manage investigator sites from initiation to close-out.
• Conduct site visits and maintain data integrity.
• Build relationships with site staff to meet clinical metrics.

Connaissances

Investigator Site Management

Monitoring Visits

ICH-GCP Guidelines

Regulatory Requirements

Formation

Degree in Healthcare

Equivalent Experience

Description du poste

Preferred location : Paris area, Toulouse, Lyon, or potentially other big cities in France

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical and biotechnology organizations.

With our patients at the center of all we do, we help accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures excellence in what we do.

Our Biotech Solutions Department offers Clinical Research Associates in France a supportive and collaborative environment, with opportunities to gain a wide range of therapeutic experience. We emphasize a flexible and adaptable approach to meet our clients’ needs.

Our Clinical Delivery Department is world-class, providing significant opportunities for career growth through internal training, promotion pathways, mentoring, and employee recognition.

As a Clinical Research Associate at ICON, you’ll work in a large, fast-paced environment alongside a team of highly qualified CRAs to identify, select, initiate, and close out investigational sites for clinical studies in phases I - IV, ensuring compliance with applicable regulations and ICH-GCP principles.

Key responsibilities :

• Managing investigator sites for assigned studies from initiation to close-out.
• Planning and conducting site visits (feasibility, selection, interim, close-out) as per the monitoring plan.
• Building effective relationships with site staff to meet clinical metrics.
• Attending investigator meetings, managing clinical supplies, and following up on drug safety issues.
• Maintaining data integrity through diligent site tracking and adherence to guidelines.

You will be an integral part of a global study team, playing a key role in our clients’ drug development processes.

The Requirements

To succeed in this role, you will need :

• Experience in investigator site management, including monitoring visits, from a pharmaceutical or CRO environment.
• Knowledge of ICH-GCP guidelines and regulatory requirements.
• Education to degree level, equivalent experience, or licensure as a healthcare professional.

Benefits of Working at ICON :

We prioritize building a culture that rewards high performance and nurtures talent. Our salary packages are competitive and benchmarked regularly. We offer annual bonuses based on performance, comprehensive health benefits, retirement plans, and other perks.

Beyond compensation, we foster an environment where you can find purpose and make a lasting impact.

ICON is an equal opportunity employer, committed to a workplace free of discrimination and harassment. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

If you need a reasonable accommodation during the application process or to perform job functions, please inform us through the provided form.

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Position: Clinical Research Associate • Strasbourg