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Senior CRA

Posting Locations BE | NL
Posted Date 21 hours ago(7/30/2025 8:28 AM)
ID
2025-120981

Overview

Job Title: Clinical Research Associate (CRA)
Location: [Insert Location]
Travel Requirement: Up to 60% (Domestic and International)

 

Summary:
We are seeking a dedicated Clinical Research Associate (CRA) to join our team. In this role, you will be responsible for identifying, initiating, monitoring, and closing investigational sites for clinical studies. You will ensure that all activities align with the study protocol, ICH-GCP guidelines, applicable regulations, and ICON's Standard Operating Procedures (SOPs). You will also help mentor and support less-experienced team members, serving as a benchmark for monitoring excellence.

Responsibilities

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

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.

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