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The Methodist Research Institute
Location: Houston, TEXAS
Posted: 02/14/2013
Refreshed: 05/23/2013
Application deadline: None
Type: Full time
Career Level: Not specified
Salary Range: Not specified
Number of Jobs: 1
Relocation Available: No
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Industries
Healthcare
Description
Description: JOB SUMMARY Coordinates complex research projects that may involve sites and/or the supervision of research activities. Implements research protocols, including screening and enrolling subjects, obtaining blood and other specimens for tests. Administering medications and maintaining pertinent patient records. Obtain, record, validate and interpret data to achieve the goals of the research project. Serves as a liaison between physicians, patients, staff and sponsors.
PATIENT AGE GROUP SERVED Direct patient care.
DUTIES AND RESPONSIBILITIES 'Serve as Study Coordinator for cardiology/cardiovascular clinical trials (as indicated), managing study recruitment in a clinical setting to maintain patient recruitment goals. 'Complete case report forms and ensure that data is accurate and complete. 'Performs device accountability, and maintains inventory of study related supplies in appropriate areas. 'Prepare presentations to schedule institutional training for physicians, nurses and staff on research protocol. 'Provide patient education regarding disease process and involves patient and family in decision making processes. 'Generates reports for supervisor on patient enrollment and tracking of assigned research studies. 'Maintains accountability of own ongoing professional growth and development. 'Performs nursing functions as approved by hospital administration for the conduct of clinical research. 'Maintains strict confidentiality of patients, employees and hospital information at all times. 'Responsible for completion of case report forms and reporting of adverse events to sponsor. 'Responsible for accountability logs for study product/device. 'Performs other duties as assigned. EDUCATION REQUIREMENTS 'Associate Degree in Nursing required 'Bachelors Degree preferred
EXPERIENCE REQUIREMENTS 'Minimum of 1 year of experience required 'Minimum of 2 years of full-time experience coordinating clinical trials required.
CERTIFICATES, LICENSES AND REGISTRATIONS REQUIRED 'Current Registered Nurse Licensure in the State of Texas
SPECIAL KNOWLEDGE, SKILLS AND ABILITIES REQUIRED 'Supervisory experience required. 'Requires highly effective communication skills. 'Requires highly effective time management skills 'Requires ability to understand and implement protocols. 'Requires experience with computer database management. 'Requires Microsoft Office skills. 'Requires strong interpersonal skills.
PHYSICAL REQUIREMENTS 'Extended periods of walking and standing may be required. 'Lifting, pushing or pulling required (minimum 50 lbs.) 'An Activity Checklist (see final page)
WORKING ENVIRONMENT Patient care unit conditions Universal precautions required Significant potential for exposure to Latex
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