CRA II: Ophthalmology Trials | Global Travel

KCR Placement; Pennsylvania; On-site; USD 80,000 - 110,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II for the Northeast region in the United States. You will design and analyze clinical trials, monitor sites, ensure data integrity, and contribute to study documentation. Experience in Ophthalmology trials or multi-TA is preferred.

You will conduct site qualification, initiation, monitoring, and close-out visits, collaborate with investigators, resolve data queries, and support regulatory compliance while traveling ~60% to sites.

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.
• 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%).

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

Organizational skills

Communication

Attention to detail

Independence

Travel willingness

Education

Bachelor's degree

CRA experience (2+ years)

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II for the Northeast region in the United States. You will design and analyze clinical trials, monitor sites, ensure data integrity, and contribute to study documentation. Experience in Ophthalmology trials or multi-TA is preferred.

You will conduct site qualification, initiation, monitoring, and close-out visits, collaborate with investigators, resolve data queries, and support regulatory compliance while traveling ~60% to sites.