Senior CRA II — Travel‑Ready Clinical Trials

ICON San Antonio; New York (NY); In loco; USD 65.000 - 95.000; Tempo pieno

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Research Associate II to support sponsor-dedicated trials across NY, NJ, PA and MA. You will design and monitor clinical trials, interpret complex data and contribute to advancing innovative therapies.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance and data integrity, collaborate with investigators, review data queries, and help prepare study documentation.

Competenze

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 1 year 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 as required (approximately 60%)
• Must be located in PA, NY, NJ, MA, ME, VT, NH, CT, RI

Mansioni

• 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 facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Conoscenze

Clinical trial monitoring

ICH-GCP knowledge

Communication skills

Organizational skills

Travel readiness

Formazione

Bachelor's degree in science/healthcare

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Research Associate II to support sponsor-dedicated trials across NY, NJ, PA and MA. You will design and monitor clinical trials, interpret complex data and contribute to advancing innovative therapies.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance and data integrity, collaborate with investigators, review data queries, and help prepare study documentation.