Study Start Up Associate (ICF Reviewer) - REMOTE
About the role
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- Perform feasibility, site identification, site contract negotiation, and other study start up activities, as assigned.
- Prepare, review and submit submissions to ethics and regulatory and other relevant authorities in order to obtain all necessary authorizations/approvals pertaining to the clinical trial conduct.
- Perform timely and accurate data entry of regulatory documents, submission status and maintenance of Country/Investigator information in the appropriate clinical trial management system.
- Minimal travel may be required (10%)
- A high school diploma or local equivalent
- Bachelor’s Degree preferably in Life Sciences
- Minimum of 1 years’ experience or understanding of clinical study starts up requirements and activities.
- Experience of Clinical Trial operations
- Experience meeting regulatory and ICON guidelines
- Proficient project management skills.
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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