ICON Careers: Step Into a Rewarding Clinical Research Associate Role
If you’re exploring growth-oriented opportunities through ICON careers, the Sr Clinical Research Associate position is an excellent pathway. ICON, a global leader in healthcare intelligence, offers a dynamic environment where your expertise in clinical trials can shine. This role is ideal for professionals seeking a strong foundation in a clinical research associate job, while contributing to future-driven healthcare jobs that advance medical innovation.
Job Position: Sr Clinical Research Associate / Clinical Research Associate II (CRA II)
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization known for shaping the future of medical development. Through ICON careers, the company promotes inclusion, talent growth, and innovation. As a global leader in healthcare jobs, ICON supports professionals who want to contribute to transformative clinical research and high-impact studies.
Qualifications:
- Bachelor’s degree in a healthcare-related field.
- Minimum 2 years of experience as a Clinical Research Associate.
- Strong understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
- Excellent communication and organizational skills with attention to detail.
- Ability to work both independently and collaboratively.
- Willingness to travel at least 60% (domestic and international) with a valid driver’s license.
These qualifications position you strongly within the competitive landscape of ICON careers and broader healthcare jobs.
 ICON Careers Job Description:
This position under ICON careers allows you to take on a vital part in designing and analyzing clinical trials, interpreting medical data, and supporting new treatments. As part of a growing field of healthcare jobs, this clinical research associate job gives you the opportunity to work in a fast-paced and meaningful environment.
Key Responsibilities:
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to support smooth study conduct.
- Performing data review and resolving queries to ensure high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
These responsibilities align with the core expectations of a clinical research associate role in global healthcare.
