ICON plc is a world-renowned clinical research organization (CRO) known for delivering comprehensive solutions to biopharmaceutical and medical device companies. With operations spanning over 40 countries, ICON focuses on accelerating the development of new treatments through innovative research and clinical trials.
Working at ICON means becoming part of a dynamic, forward-thinking team that pushes the boundaries of clinical research excellence while delivering value to clients and advancing healthcare outcomes globally.
Job Responsibilities of a Clinical Research Associate (CRA)
In this position, the Clinical Research Associate will be involved in the following tasks:
- On-site monitoring and management of clinical trials in oncology and other therapeutic areas across the UK.
- Ensuring compliance with ICH-GCP guidelines and regulatory requirements at study sites.
- Conducting pre-study, initiation, monitoring, and close-out visits for assigned studies.
- Collaborating closely with site staff to ensure data accuracy and proper documentation.
- Identifying and resolving site issues to maintain the smooth execution of clinical trials.
- Maintaining high standards of patient safety and data integrity throughout the research.
- Reporting progress and communicating updates effectively with the project team and sponsor.
Qualifications and Experience Required for the Role
To be eligible for this role, you must meet the following requirements:
- 2+ years of experience in on-site monitoring, specifically in oncology clinical trials or related therapeutic areas.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and clinical trial protocols.
- Bachelor’s degree in life sciences, pharmacy, or a related field.
- Valid work permit for the UK (mandatory).
- Previous experience working within a sponsor-dedicated model is an advantage.
Skills for a Successful CRA
The ideal candidate for this Clinical Research Associate role should possess the following key skills:
- Strong communication and interpersonal skills to liaise with study sites and sponsors effectively.
- Exceptional organizational and time management abilities to handle multiple tasks efficiently.
- Familiarity with clinical trial software and documentation tools.
- Analytical thinking to identify and resolve site-related challenges.
- Attention to detail to ensure compliance with protocols and data quality.
- A passion for advancing healthcare through clinical research.
How to Apply for the Clinical Research Associate Position at ICON plc
If you meet the qualifications and are eager to explore this exciting opportunity, here’s how you can apply:
- Send your CV along with a cover letter detailing your relevant experience to:
Gayathri.Nareshkumar@iconplc.com - Mention “CRA Application – Oncology Expertise” in the subject line of your email.
- Ensure that your application highlights your on-site monitoring experience and therapeutic area expertise.
- Early applications are encouraged, as the position is expected to attract a high volume of applicants.
