Senior CRA
About the role
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As a top 5 CRO in the world, we are looking to strengthen our Clinical Operations team in the UK. We empower our CRA's to work independently and enthusiastically to balance all necessary activities required.
As a Senior Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – III, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
· Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
· Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
· Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
· Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
· Dependent on level of experience you may assist in training and mentoring less expert CRA’s and/or lead CRA’s working on international projects
· 18 months+ of monitoring experience in phase I-III trials as a CRA
· Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
· You will possess excellent written and verbal communication in English
· Ability to produce accurate work to tight deadlines within a pressurized environment
· You will be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
Other than working with an outstanding team of ambitious people, we also offer a very competitive compensation package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
Following your application, you will be contacted by one of our dedicated recruiters and if successful, we will be able to provide you with more details about this opportunity.
ICON is an equal opportunity employer - M/F/D/V and committed to delivering a workplace free of any discrimination or harassment.
EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
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