Clinical Job Opportunity at ICON | Apply Now
Clinical job seekers looking for exciting opportunities in the clinical research industry can explore this excellent opening at ICON plc. ICON careers offer professionals the chance to work in a world-leading healthcare intelligence and clinical research organization. This life sciences job in Spain is ideal for candidates interested in clinical monitoring, site management, and supporting high-quality clinical trials in a dynamic hybrid work environment.
- Job Position: Clinical Site Associate
- Location: Barcelona, Madrid
- Job Reference: JR143319
- Department: Clinical Monitoring
About the Company
Clinical role opportunities at ICON plc provide candidates with exposure to one of the world’s leading healthcare intelligence and clinical research organizations. ICON careers are known for fostering innovation, inclusion, and excellence while helping shape the future of clinical development globally. The company offers a collaborative work environment, competitive employee benefits, and professional growth opportunities for individuals pursuing a life sciences job in the clinical research sector.
Clinical Job Description
Clinical role responsibilities at ICON include supporting site management activities and ensuring clinical trials are conducted efficiently, compliantly, and according to quality standards. The Clinical Site Associate will collaborate with Clinical Research Associates (CRAs), site staff, and cross-functional teams to support study start-up, maintenance, and close-out activities.
This life sciences job involves maintaining clinical trial documentation, supporting site communications, coordinating logistics, and contributing to process improvements within the organization.
Qualifications
Clinical job applicants interested in ICON careers should meet the following qualifications:
- Bachelor’s degree in life sciences or a related field, or equivalent experience.
- Initial experience in clinical research, administration, or a regulated environment preferred.
- Strong organizational and multitasking skills.
- High attention to detail and accuracy in documentation and data entry.
- Effective written and verbal communication skills.
- Proficiency in MS Office and electronic systems/databases.
- Ability to work collaboratively and adapt to changing priorities.
Key Responsibilities – Clinical Job
Clinical role duties include:
- Supporting site activation activities, including collection, review, and tracking of essential documents and approvals.
- Maintaining updated site information and status in clinical trial management systems and trackers.
- Assisting CRAs and project teams with site communications and resolution of site-level queries.
- Coordinating logistics for site visits and meetings, including scheduling and documentation preparation.
- Ensuring accurate filing and maintenance of essential documents for audit and inspection readiness.
- Collaborating with internal stakeholders to support site payment processing and issue resolution.
- Contributing to process improvement initiatives and sharing best practices to enhance efficiency.
Why Choose ICON Careers?
Clinical job opportunities at ICON plc allow professionals to work in an inclusive and diverse workplace focused on innovation and employee well-being. ICON careers provide strong career development opportunities for candidates looking to build a successful future in clinical research and life sciences jobs globally.
The company encourages candidates to apply even if they do not meet every requirement, offering equal opportunity employment and a workplace free from discrimination and harassment.
