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Protocol Coordinator - Advancing Military Medicine Organization (Dwight, KS) in Manhattan, Kansas For Sale

Type: Technical, For Sale - Private.

Responsibilties:Interview research subjects for protocols, and collect and analyze data to validate eligibility and patient commitment. Review patient records and screens research subjects for eligibility for participating in research protocol.Administer appropriate drugs/devices/infusions to research subjects as necessary. Draw blood and obtain other specimens as required.Identify problems in the research design or analysis methodology and trends in research subject reactions to treatment. Collect, organize, catalog, disseminate and maintain appropriate files of current data. Determine whether data is clinically significant. Report results that warrant prompt action immediately to the COR, government clinical investigators, appropriate physicians, and other government officials as designated by the COR or as appropriate based on the situation.Educate patients and research subjects about the research protocol, their roles in the protocols, and other vital information. Act as a case manager for the research subjects.Adhere to the legal, professional, and ethical codes with respect to confidentiality and privacy. Assure that protocol requirements are achieved within GCP. Conduct counseling sessions for patients/research subjects and informs them of their rights and responsibilities.Travel to/from assigned workplace to support protocols as needed. Schedule patients/research subjects for appointments.Determine what needs to be done to include the assessment of unusual circumstances and variations in approach and identify and respond to incomplete or conflicting data. Interpret all data, plan all work and refine methods and techniques used, as applicable.Ensure implementation of appropriate protocol requirements, registration, report and follow-up.Develop, document and submit quarterly compliance reports to the COR.Coordinate communication/actions between government review boards, educational institutions, private companies and the Director of Trauma Research.Adhere to all hospital policies and procedures, Joint Commission regulations, and National Patient Safety Goals.Maintain weekly/monthly status reports on all research subjects. Act as a liaison between research subjects and physicians. Observe the research subjects for improvements, set-backs and changes in conditions.Perform quarterly quality assurance audit of a minimum of 10% of studies being conducted. Audit findings and recommendations for process revisions will be provided to the COR and any other government official as designated by the COR.Performs other duties as needed.Required Knowledge, Skills, and Abilities: Knowledge of procedures and techniques necessary for performing a variety of clinical research tasks. Ability to utilize medical knowledge to interpret diagnostic codes, test results, and clinical notes. Skilled in the use of MS Word, Excel, email, and Power Point. Skilled in multi-tasking, writing memorandums, letters and correspondence. Ability to work well in a large group with both internal and external investigators, collaborators, consultants, field experts, research staff and team members, as well as sponsors. Ability to work independently, to plan and prioritize work with minimal supervision, be productive and produce quality results, and exercise good judgment. Minimum Education/Training Requirements: Licensed Practical Nurse, Associate’s Degree in Nursing, Physician Assistant, Physical Therapist, Occupation Therapist, or Bachelors degree in health related field. Master’s or PhD is preferred.Minimum Experience: 2-4 years clinical healthcare experience with at least 1 year in clinical research.Physical Capabilities: Long periods of sitting and standing; some bending, lifting, and walking; escorting patients and carrying light items; may encounter patients who are confused, agitated, or abusive. Must be able to travel to local sites for patient recruitment.Required Licenses, Certification or Registration: Licensed in respective field in one of the 50 U.S. States or Territories, certified in basic cardiac life support. Certified as a Clinical Research Coordinator (CCRC) or Clinical Research Associate (CCRA) preferred. Required to pass a National Agency Check (NAC).Supervisory Responsibilities/Controls: Supervisors and/or provides guidance to junior staff.Work Environment: Laboratory, office or clinical/hospital environment; possible evening and/or weekend hours.
Source: http://www.jobs2careers.com/click.php?id=xxxxxxxx22.96

State: Kansas  City: Manhattan  Category: Technical
Technical in Kansas for sale

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