| Informed Consent Coordinator -- Cincinnati, OH |
Author: Patricia MacCubbin
Date: 06-01-11 15:24
Schulman Associates IRB is hiring! In addition to offering a challenging and rewarding work environment, we also offer a generous benefits package suitable for the diverse needs of our employees. Please review the following details for a position summary. For more information about this position and to apply, please visit our website at:
http://www.sairb.com/SitePages/OurCompany/careers.aspx .
POSITION SUMMARY: This position provides support for the Board during and after review of study-related materials (protocols, amendments, informed consent documents and other relevant documents); serves as a liaison between the Board and Sponsor/Contract Research Organization (CRO)/Site; relays Board communication regarding new research studies to the appropriate parties.
PRIMARY RESPONSIBILITIES:
•Review clinical trial protocols, amendments, informed consent documents and other relevant study-related items, as assigned.
•Attend Board meetings.
•Develop and edit informed consent documents;
•Act as a liaison with the Board, sponsors, sites and CROs;
•Engage with Team members to dynamically assess process and maximize improvement opportunities.
REQUIRED KNOWLEDGE/SKILLS/ABILITIES:
•BA/BS required
•2 years in health-related field or clinical research required, 5 years preferred
•Experience in clinical trials;
•Excellent communication skills (written and verbal); writing samples are required;
•Detail-oriented, self-directed approach to work and an ability to work well in a fast-paced environment.
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