Senior CRA
About the role
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Are you ready to be a part of a successful study delivery team? ICON's award-winning study execution capabilities have led to the approval of 18 of the world's top 20 best-selling drugs. Make your experience count for the benefit of patients worldwide. www.iconplc.com
Role Responsibility
Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II - III ensuring that applicable regulations and principles of ICG-GCP are adhered to 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
36 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 Native local language and conversational English is a must 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 pressurized environment.
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits 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.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
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
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