Clinical Research Associate 1

ICON; Antwerpen; Hybride; EUR 45 000 - 65 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme (

Résumé du poste

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a CRA I at ICON, you will contribute to our clinical trial operations function, delivering high-quality monitoring outcomes across your programmes.

Your role includes coordinating study setup and monitoring, running sponsor queries, and supporting study feasibility and documentation. You will build strong relationships with investigators and staff while ensuring patient safety and regulatory compliance.

Qualifications

• Requires knowledge of ICH-GCP guidelines and ability to review medical data.
• Excellent written and verbal communication in English.
• Good social skills enabling timely handling of queries.
• Willingness to travel approximately 60% of the time.

Responsabilités

• Deliver clinical trial monitoring work to a high standard.
• Coordinate setup and monitoring activities with the team and stakeholders.
• Run sponsor-generated queries and support study cost efficiency.
• Develop and maintain strong relationships with investigators and site staff.
• Ensure patient safety by complying with ICON procedures and regulatory requirements.

Connaissances

ICH-GCP knowledge

English proficiency

Communication skills

Team collaboration

Willingness to travel

Formation

University degree in medicine, science, or equivalent

Description du poste

Clinical Monitoring - Site Management

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Willingness to travel as required (approximately 60%)

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here