Life Sciences Job at ICON | Apply Now
Life sciences job opportunities in Europe are expanding rapidly, and this Clinical Site Associate position at ICON in Prague offers an excellent entry into clinical research. If you’re looking to build a career in clinical trials, site management, and healthcare innovation, this role provides hands-on experience in a globally recognized organization.
- Job Title: ICON Clinical Site Associate
- Location: Prague
- Job ID: JR149189
- Department: Clinical Monitoring
About the Company
Life sciences job seekers exploring ICON careers will find ICON plc to be a world-leading healthcare intelligence and clinical research organization. The company fosters an inclusive environment that drives innovation and excellence, with a mission to shape the future of clinical development. ICON is known for delivering high-quality clinical trial solutions globally while supporting employee growth and well-being.
Job Description
Life sciences job roles like this Clinical Site Associate position involve supporting site management activities and ensuring clinical trials are conducted efficiently, compliantly, and with high-quality standards. This clinical job is ideal for candidates interested in scientific operations and clinical research coordination.
As a Clinical Site Associate at ICON, you will contribute to scientific operations activities, take responsibility for deliverables, and collaborate with cross-functional teams to support clinical trial success.
Qualifications
Life sciences job qualifications for this role ensure candidates can thrive in a regulated clinical environment:
- Bachelor’s degree in life sciences, healthcare, or a related field
- Initial experience in clinical research, administration, or a regulated environment preferred
- Strong organizational skills with the ability to manage multiple tasks and deadlines
- High attention to detail in documentation and data entry
- Effective communication skills with a customer-focused approach
- Proficiency in MS Office and electronic systems
- Ability to work collaboratively in a team environment
- Willingness to travel approximately 10%
Key Responsibilities
Life sciences job responsibilities in this role focus on clinical trial support and coordination:
- Supporting site activation activities, including collection, review, and tracking of essential documents and approvals
- Maintaining up-to-date site information in clinical trial management systems and trackers
- Assisting CRAs and project teams with site communications and resolving site-level queries
- Coordinating logistics for site visits and meetings, including scheduling and documentation
- Ensuring accurate filing and maintenance of essential documents for audit readiness
- Collaborating with internal stakeholders for timely site payment processing
- Contributing to process improvement initiatives and sharing best practices
Why Join ICON?
Life sciences job seekers looking for life science jobs in Europe will benefit from ICON’s employee-focused culture. The company offers competitive salaries and a comprehensive benefits package designed to support work-life balance and well-being.
Key benefits include:
- Annual leave entitlements
- Health insurance options for employees and families
- Retirement planning programs
- Global Employee Assistance Programme (LifeWorks)
- Life assurance coverage
- Flexible benefits like childcare vouchers, gym memberships, and travel subsidies
