🚀 Launch Your Clinical Research Career: Clinical Site Associate (CSA)
Join ICON plc, a world-leading healthcare intelligence and clinical research organization, as a Clinical Site Associate (CSA). This is your foundational on-site role where you will provide vital operational support for the execution and management of clinical trials, directly contributing to the advancement of innovative medical treatments. You will gain hands-on experience in clinical operations, building the essential skills for a successful career in clinical development.
We are seeking a proactive, detail-oriented individual to support our clinical trial activities. If you are passionate about healthcare, excel in organized environments, and are eager to learn the intricacies of clinical research, this is your opportunity to start a rewarding career with a global industry leader.
🎯 Your Clinical Operations Support Mission: Key Responsibilities
Trial Execution & Site Coordination
- Assist in the planning, initiation, and execution of clinical trial activities, ensuring alignment with study timelines and objectives.
- Coordinate closely with investigative sites to facilitate compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
- Conduct site feasibility assessments and participate in the site selection process to help identify high-performing clinical trial locations.
Study Monitoring & Data Quality Support
- Support the monitoring of study progress and data collection activities to help ensure data quality, accuracy, and timely entry.
- Assist in the preparation, collection, and review of essential study documentation, including regulatory submissions, reports, and Trial Master File (TMF) deliverables.
Administrative & Operational Support
- Serve as a key liaison between Clinical Research Associates (CRAs), investigative sites, and internal cross-functional teams.
- Help maintain study trackers, schedule meetings, and manage communication to ensure smooth trial operations.
- Contribute to process improvement initiatives to enhance the efficiency and quality of site management activities.
⭐ Your Profile: Clinical Site Associate Qualifications
Essential Requirements
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field.
- Previous experience or a strong interest in clinical research is preferred. This role is ideal for recent graduates or professionals seeking to enter the field.
- Strong organizational skills and meticulous attention to detail.
- Ability to work on-site as required (#LI-Onsite).
Core Competencies
- Excellent Communication Skills: Clear verbal and written communication abilities for effective collaboration with sites and internal teams.
- Proactive & Adaptable: Ability to work both independently and as part of a team in a fast-paced, dynamic environment.
- Effective Prioritization: Skill in managing multiple tasks, prioritizing workload, and meeting deadlines.
- Tech-Savvy: Proficiency in Microsoft Office Suite and the ability to learn new clinical systems quickly.
Career Pathway
- This role is designed as a stepping stone into clinical operations, with a clear path for advancement to roles such as Clinical Trial Assistant (CTA), In-House CRA (IHCRA), or Clinical Research Associate (CRA).
💫 Why Build Your Career as a CSA at ICON?
Gain Foundational Clinical Research Experience
- Receive comprehensive training in ICH-GCP, clinical trial processes, and regulatory standards.
- Gain hands-on, practical experience that will form a solid foundation for a long-term career in clinical development.
On-Site Collaboration & Team Support
- Work on-site within a collaborative team environment, learning directly from experienced clinical operations professionals.
- Join a diverse, inclusive, and supportive culture that values your growth and nurtures talent.
Competitive ICON Benefits
- Attractive entry-level salary and benefits package.
- Comprehensive health insurance offerings for you and your family.
- Generous annual leave entitlements.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme (EAP) providing 24/7 support.
- Clear pathways for professional development and career advancement within a global organization.
✨ Ready to Become the Operational Backbone of Clinical Trials?
If you are a motivated, detail-focused individual looking to start a meaningful career in clinical research, we encourage you to apply. This Clinical Site Associate role offers the perfect platform to learn, contribute, and grow within the vital field of clinical development.
Apply Now and take the first step in your clinical research career with a global leader.
