Clinical Research Coordinator at Cayuga Health System Ithaca, NY

Benefits

Qualifications

• •A Clinical Research Coordinator needs to have strong organizational skills along with the ability to think on their feet when faced with new situations that arise throughout each day within a professional medical environment
• •Effective problem solving and critical thinking skills with meticulous attention to detail
• •Demonstrated ability to work as a team as well as independently in a fast-paced environment
• •Ability to work flexible hours
• •Bachelor's degree or 2-4 years of direct clinical research experience; or equivalent combination of education and experience, are required
• •Possess working knowledge of the Title 21 Code of Federal Regulations (CFR), International Conference of Harmonization (ICH) and Good Clinical (Research) Practice (GCP) Guidelines, or ability to complete related training within 15 days of hire
• •Both standing, sitting and lifting of lab supplies
• •Physical demands of this position include: vision, hearing, repetitive motions and environment
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Responsibilities

• •Work directly with Physician Investigators and Clinical Research Nurses on implementing clinical research being performed onsite
• •Involved in all aspects of clinical trial coordination including: study activation support, subject recruitment, detailed data entry, subject visits, follow-up, regulatory documentation, and coordination/preparation for monitor visits
• •Scheduling and overseeing subject visits according to protocol and completing detailed documentation of study activities, including preparing clinical data for the Investigator to determine response and clinical outcomes
• •Administrative administrator duties such as scanning, faxing, calendar management, organizing supplies (lab kits), etc
• •May support budget process for clinical trials, as needed, and assist is tracking study charges and invoicing
• •Report directly to the Program Manager and will have additional obligations and responsibilities as assigned by the Research Program Medical Director and Regulatory Affairs Consultant
• •Strong interpersonal and communication skills
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