Clinical Research Associate II — Global Trials & Data
ICON Strategic Solutions
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Benefits offered by this job
Job summary
ICON Strategic Solutions seeks a Clinical Research Associate II to contribute to sponsor-dedicated trials with ICON’s global expertise. The role involves monitoring activities, data review, and collaboration with investigators to advance clinical research and patient benefit worldwide.
Responsibilities include site visits, ensuring data integrity and protocol compliance, and assisting in study documentation.
Qualifications
- Minimum 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 approximately 60%.
Responsibilities
- 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
Skills
Education
Job description
ICON Strategic Solutions seeks a Clinical Research Associate II to contribute to sponsor-dedicated trials with ICON’s global expertise. The role involves monitoring activities, data review, and collaboration with investigators to advance clinical research and patient benefit worldwide.
Responsibilities include site visits, ensuring data integrity and protocol compliance, and assisting in study documentation.
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