Senior CRA

Key Responsibilities:

• Select, initiate, and manage clinical investigational sites from start-up to close-out.

• Conduct pre-study, initiation, monitoring, and closeout visits in accordance with ICON and sponsor SOPs.

• Ensure compliance with study protocols, GCP, and applicable regulations.

• Maintain and update clinical systems to ensure accuracy and timeliness of data.

• Support patient recruitment by collaborating closely with investigators and motivating sites.

• Manage regulatory documentation, including ethics/IRB submissions and approvals.

• Oversee investigational product (IP) accountability, storage, and compliance at the site level.

• Address and resolve site and sponsor-generated queries in a timely manner.

• Maintain thorough study files and ensure proper archiving upon study completion.

• Provide regular updates to the Project Manager and contribute to study progress reports.

• Support feasibility assessments, protocol development, and other study documents as needed.

• Participate in data review activities and ensure data quality and integrity.

• Train and mentor junior team members and contribute to team development.

• Assist with business development activities and represent the company when appropriate.

• Perform other duties as assigned by the Project Manager.

Qualifications:

• Strong working knowledge of ICH-GCP, clinical trial regulations, and ICON SOPs.

• Prior experience as a CRA or equivalent role in clinical monitoring.

• Familiarity with clinical trial systems and site management processes.

• Excellent organizational and communication skills.

• Independent, proactive, and solution-oriented approach to work.

• Ability to travel up to 60% (domestic and international).

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field preferred.

Why Join Us?

At ICON, we value our people and their contributions. We foster a culture of performance, innovation, and collaboration. If you're looking to grow your career in a supportive and dynamic environment while making a meaningful impact in clinical research, we encourage you to apply.