Dynamic Clinical Research Associate II | Trials & Data

KCR Placement; Center Square (PA); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyze clinical trials, interpreting complex medical data to advance innovative treatments. The role involves monitoring activities and collaboration with investigators to ensure data integrity and patient safety.

The CRA II will conduct site qualification, initiation, monitoring, and close-out visits, and support study documentation in a fast-paced, sponsor-dedicated environment.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Willingness to travel approximately 60% of the time.

Responsabilités

• 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.

Connaissances

Clinical monitoring

Site visits

Data review

ICH-GCP

Travel 60%

Formation

Bachelor's degree

Description du poste

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyze clinical trials, interpreting complex medical data to advance innovative treatments. The role involves monitoring activities and collaboration with investigators to ensure data integrity and patient safety.

The CRA II will conduct site qualification, initiation, monitoring, and close-out visits, and support study documentation in a fast-paced, sponsor-dedicated environment.