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Clinical Research Associate- can be home-based depending on experience level.
Location: Marlow

ICON have offices in Marlow and Southampton, in Southeast England, this role can be home –based or at one of these offices.

ICON Clinical Research are currently looking for experienced CRAs (with independent monitoring experience), to join our dynamic and dedicated team. As one of the top 5 CROs, we offer a flexible working environment, fantastic opportunities for career progression and to broaden your therapeutic and geographical experience. We believe that our strong foundation as a business allows us to continue hiring the best talent from the market place and with a clear vision of where we are heading is an ideal and exciting time for people to come on board.

Role Responsibility
 
Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring that applicable regulations and principles of ICH-GCP are adhered to
 
Additional Responsibilities:
 
Working independently and proactively to coordinate all necessary activities required 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
Managing sponsor generated queries efficiently and responsible for study cost effectiveness
Dependent on level of experience you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects    

Experience and Qualification
 
With a University degree in medicine, science, or equivalent, you will have previous monitoring experience in medium sized studies including study start up and close out (for all roles above Entry Level). In addition, you will also require:
 
You will have knowledge of ICH GCP guidelines and expertise to review and evaluate medical data
Fluent in English as well as the local language
Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
Ability to produce accurate work to tight deadlines within a pressurised environment
Computer literate with Microsoft Office
Must be available to travel international and domestic at least 60% fly and drive and should possess a valid driving licence.
 
 
You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.
 
Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive compensation and an exceptional benefits package
 
ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.
To apply for this role please apply directly to the ICON website

http://www.iconplc.com/careers/job-opportunities/