Site Management Associate I

ICON plc; Warszawa; Hybride; PLN 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Country-specific benefits and family-f

Résumé du poste

ICON Strategic Solutions in Warsaw, Poland, is seeking a Site Management Associate I (Regulatory) to support management of clinical trial sites and ensure regulatory compliance in a sponsor-dedicated setup.

You will assist with site monitoring activities, maintain documentation, and help deliver high standards of operational efficiency in line with study protocols and GCP guidelines.

Qualifications

• Bachelor's degree in a life sciences, healthcare, or clinical research field.
• Some experience in clinical research, site management, or related admin roles is preferred.
• Strong organizational and communication skills are essential.

Responsabilités

• Assist in monitoring clinical trial sites ensuring adherence to protocols and GCP.
• Support site management activities including documentation, data entry, and tracking metrics.
• Collaborate with cross-functional teams to address site-related issues.
• Maintain accurate records of site activities and monitoring reports.
• Participate in training to enhance knowledge in clinical trial management.

Connaissances

Regulatory knowledge

Site monitoring

GCP awareness

Organizational skills

Communication

Formation

Bachelor's degree in life sciences, healthcare administration, or clinical research

Description du poste

Site Management Associate I (Regulatory), Warsaw, Poland

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency.

What You Will Do:

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

Key responsibilities include:

• Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
• Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
• Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
• Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.

Your Profile:

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

Required qualifications and experience:

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
• Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
• Basic knowledge of clinical trial processes and regulatory requirements is a plus.
• Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.

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.

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, please let us know or submit a request here