Senior Clinical Research Associate (Site Engagement)

Posted Yesterday
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Mechelen
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
As a Senior Clinical Research Associate, you will manage clinical trial sites, ensuring compliance with protocols, conducting site visits, and providing training and support to staff.
Summary Generated by Built In
Senior CRA I Site Engagement I Belgium

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

Job Advert Posting

For our client in the Antwerp region, we are looking for a Clinical Research Associate (CRA) (Site Manager) to join our ICON team! You will be working for one of the most attractive employers in Belgium, creating a real impact on the health of patients worldwide.

As a CRA your main responsibilities will be to provide trial coordination and site management services for your assigned studies/sites. For this you will independently ensure that your sites are inspection read at all times, perform pretrial assessment,site selection, subject recruitment and retention planning, site initiation, monitoring and close-out.


What You Will Be Doing: 
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.


Your Profile:
  • Degree in a health or sciences related field

  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. 

  • Proven experience in on-site monitoring of clinical studies.

  • Demonstrated proficiency in problem solving, juggling multiple priorities and a commitment to quality and customer focus. 

  • Proven ability to work independently in a fast-paced environment. 

  • Strong communication, interpersonal, and organizational skills. 

  • Must demonstrate good computer skills.

  • Fluently Dutch, French and English

#LI-Hybrid

#LI-VV1

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Top Skills

Good Clinical Practice (Gcp)
Ich Guidelines
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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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