Study Start Up Associate I ( Informed Consent Forms )

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?   We are looking for passionate, resilient, and inspiring individuals to join our team. As a member of the Study Start-Up Team, you will play an integral role in coordinating clinical trial start-up activities and serve as the primary contact for investigators and research coordinators in corporate sponsored human clinical trials.   The role 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%)    What you need 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. Reference: 052875
Salary Range: NA
Minimum Qualification
Less than 5 years

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