Clinical Research Associate

Clinical Research Associate (all levels), Remote, 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 organization, 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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Your Profile:

• Bachelor’s degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 40%).

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 benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family. Benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings
• Competitive retirement planning offerings
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of 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

ICON is committed to Inclusion & Belonging and providing an inclusive and accessible environment for all candidates. 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 you need a reasonable accommodation for any part of the application process, please let us know.

If you are interested in the role, but unsure if you meet all of the requirements, we encourage you to apply anyway. There’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Location

Warsaw, Gdansk

Reference: JR163238

Categories: Clinical Monitoring

Remote Working: Remote

Description

We are currently seeking a Senior/Clinical Research Associate (remote based or hybrid) to join our diverse and dynamic team. As a Senior/CRA at ICON Plc, you will play a critical role in overseeing clinical trials to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do:

• Design and oversee clinical trial activities to ensure high-quality outcomes.

• Manage site qualification, initiation, monitoring, and close-out visits.

• Ensure protocol compliance, data integrity, and patient safety.

• Collaborate with investigators and site staff to facilitate study conduct.

• Review study documentation, including protocols and clinical study reports.

• Location options include Germany, France, Canada, Norway, and other regions, with remote working possibilities.