- Location
- Bulgaria, Sofia · Spain, Madrid · Poland, Warsaw · Spain, Barcelona
- Workplace
- Onsite
- Type
- Full-time
- Department
- Management
- Seniority
- Entry
- Visa
- Not sponsored
- Source
- Workday
Description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Site Management Associate II with Dutch language to join our diverse and dynamic team. As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will contribute to the efficiency of clinical research operations by providing advanced support to site management teams and fostering strong relationships with site personnel.
What You Will Be Doing:
Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.
Assisting in the preparation and review of project related documents in the Investigator Site File and Trial Master File, ensuring all site activities are compliant with GCP and applicable regulations.
Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle.
Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency.
Participating in training initiatives and mentoring junior staff to support their development in clinical trial management.
Your Profile:
Bachelor’s degree in a relevant field such as life sciences, healthcare administration, or clinical research.
Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines.
Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines.
Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards.
Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams.
Excellent English and Dutch required
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
