Clinical Research Coordinator IV
1 week ago
Essential Functions and Responsibilities:
- Ensure all study requirements are documented and meet both internal and external regulations, in accordance with protocol guidelines.
- Maintain logs including tracker submissions and update the Oncore database in a timely manner, according to CTO SOPs
- Manage all patient and /or protocol data as assigned, and respond to queries in a timely fashion.
- Schedule and participate in monitoring visits and participate in MDT team program meetings; serve as a consultant/liaison for research activities.
- Develop solutions to complicated issues relating to KCI research processes and core support; then educate other CTO staff members.
Required:
- Bachelor's degree and at least four years' experience coordinating clinical trials: or equivalent combination of education/experience that includes five or more years coordinating clinical trials.
- Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role.
- Thorough understanding of Good Clinical Practice guidelines, Code of Federal Regulations, clinical trials monitoring, regulatory compliance.
- Proficient with the Microsoft suite including Excel and Power point.
- Exceptional interpersonal skills required and excellent verbal and written communication skills necessary to effectively deal with individuals both inside and outside the organization from diversified backgrounds.
- Skilled in communicating sensitive/difficult information and maintaining highly confidential information and situations.
- Demonstrated high level of interpersonal skills and analytical ability.
- Excellent writing and organizational skills
- Demonstrated leadership abilities required.
- Demonstrated initiative and attention to detail.
- Medical and/or science experience/education preferred.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
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