Job Description
Clinical Research Coordinator dutes and Responsiblities:
Plans and coordinates the initiation of research study protocol, and the establishment of operating policies and procedures. Plans, implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data. Recruits, instructs, and coordinates research subjects and/or volunteers, as appropriate to specific study objectives and work scope. Ensures the smooth and efficient day-to-day operation (as needed) of research and data collection activities; acts as the primary administrative point of contact for internal research staff and as the principle operational liaison for other research organizations, funding agencies and regulating bodies. Coordinates the day-to-day activities (as needed) of any 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. Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies. To implement quality control process throughout the conduct of the trialJob Requirements
Clinical Research Coordinator Requirements:
EDUCATIONAL REQUIREMENTS:
Minimum of a two-year degree in nursing or a four-year degree in a health care/science related field SPECIALIZED CERTIFICATES/LICENSES:
At least 2 years of experience that is directly related to the duties and responsibilities specified TRAINING/EXPERIENCE CLINICAL REQUIREMENTS:
Minimum of two years clinical research experience GCP training IATA certification (dangerous goods regulations as they pertain to biological specimens) Diabetic neuropathy or nephrology experience a plus TRANSFERABLE COMPETENCY REQUIREMENTS:
Verbal communications skills Problem-solving skills Planning/organizational skills Personal motivation Project management capabilities Customer service skills SPECIFIC TECHNICAL COMPETENCY REQUIREMENTS
Understanding of ICH/GCP guidelines for human research Understanding of Code of Federal Regulations for Human Subjects Computer Competency including proficiency in Microsoft Word and Excel Understanding Phases I-IV drug development processes ECG, phlebotomy skills, and any other technical skills related to the completion of a study visit as required by the protocol.
PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS
Work is normally performed in a typical interior/office work environment Exposure to human bodily fluids Laboratory processing and shipping procedures Subject/Patient Care Extensive Computer Use Occasional on-call night and weekend work schedules Lifting up to 20 pounds and occasionally more than 20 pounds Ability to receive notice and communicate via cell phone Ability to drive and daily availability of an automobileCountry: USA,
State: Washington,
City: Spokane,
Company: InVentiv Health.
Комментариев нет:
Отправить комментарий