Ophthalmology CRA II: Clinical Trials & Data Insight

Regulatory Jobs

Pennsylvania

On-site

USD 91,000 - 114,000

Full time

2 days ago

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Benefits offered by this job

Competitive salary

Health coverage

Retirement plan

Life insurance

Wellbeing programs

Training & development

Job summary

ICON Strategic Solutions, part of ICON, is seeking a Clinical Research Associate II for the Northeast region. In a sponsor-dedicated model, you will design and monitor trials, interpret medical data, and help advance therapies.

The role requires at least 2 years CRA experience, a scientific or healthcare degree, knowledge of ICH-GCP, and travel about 60%. Join a world-leading FSP organization that supports career development.

Qualifications

Bachelor's degree in a scientific or healthcare-related field required.
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 ~60%.

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 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.