Clinical Research Associate
- Edinburgh
- Clinical Monitoring
- ICON Full Service & Corporate Support
- Hybrid: Office/Remote
About the role
This vacancy has now expired. Please see similar roles below...
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility and Inclusion. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
Experienced England, UK-based CRA/clinical research associate required to augment existing non-Oncology CRA team, for pharmaceutical and biotechnology company company partner.
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.
You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
Amongst other tasks, your main responsibilities will be to;
- Contribute to the selection of potential investigators.
- Provide the required monitoring visit reports within required timelines
- Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
- Perform source data verification according to SDV plan and ensure data query resolution
- Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
- Train, support and advise Investigators and site staff in study related matters.
We are looking for candidates with strong experience working in a clinical research monitoring capacity, and residing in England, UK (with appropriate right-to-work in the UK already granted, if applicable)
#LI-RK1
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
Teaser label
Our PeopleContent type
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Summary
How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce
Teaser label
A Day In The LifeContent type
BlogsPublish date
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Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?
by
Suzaita Hipolito
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