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Research Coordinator

Location:Honolulu, HI
Benefits:Employer Paid Medical, Dental, Vision, etc
Employment Type:Full Time
Site:Tripler Army Medical Center
Description:The Research Coordinator will review medical records of all patients admitted to psychiatric inpatient units for indication of depression or imminent suicide risk. They will also be responsible for organizing research information, patient recruitment, scheduling, consenting, screening, and observing subjects, and assisting with data collection analysis and reporting.

The purpose of this randomized controlled trial (RCT) is to establish the effectiveness of a Caring Letters Project (CLP) to prevent suicides among Service Members and Veterans.
Duties:Principle duties and responsibilities include, but are not limited to, the following:

•Promote safety and confidentiality of research participants at all times
•Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
•Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
•Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data
•Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
•Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
•Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives
•Document all correspondence and communication pertinent to the research
•Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization
•Comply with all the rules and regulations as applicable to assigned duty station
•Create and adhere to a data quality and quality assurance plan
•Assist with interim and annual reports. S/he will be the primary liaison at the data collection site and will be responsible for explaining the project to military personnel associated with the study
•Demonstrate proficiency in performing basic study related procedures
•Complete required and applicable research training needed to complete research
•Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)
Qualifications:•Bachelors degree required
•Prior psychological experience or behavioral research preferred
•2-4 years experience in clinical research preferred
•2-4 years non-profit, research, or healthcare experience desired
•Demonstrate competence in oral and written communication
•Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor
•Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
•Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
•Knowledge of CFR, GCP and ICH guidelines

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