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MCW: SARGEANT HEALTH CENTER Clinical Research Coordinator II in MILWAUKEE, Wisconsin

JOB REQUIREMENTS: Position Description: Purpose Perform the day-to-day administrative and clinical activities related to clinical research trials. Provide support to the Principal Investigator and research team to facilitate the achievement of the program's goals. Assist with recruiting, training, and any other activity necessary for successful completion of the research trial. Primary FunctionsWorking with multiple Principal Investigators ensure proper conduct of all CTO trials at MCW, Children's Hospital of Wisconsin and Clement J. Zablocki VA Medical Center. Maintain regular contact and provide updates whenever necessary, both to PI and CTO administration.. Work closely with CTO leadership on a day-to-day basis providing updates and managing priorities. Responsible for recruitment, screening, enrollment, consenting of study participants. Coordinate research protocols including scheduling necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining regular contact with study participants Oversee the collection, analysis, and dissemination of research data. Report study data and progress to study investigators and trial sponsors. Develop, implement and maintain comprehensive databases and files related to clinical trials. Schedule, prepare for and participate in routine monitoring visits for trials. Ensure all study material and data are ready for review and in good standing Identify barriers or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators and CTO management to work towards resolution Assure compliance with relevant IRB, HIPAA, GCP and other regulatory agency requirements. Responsible for maintaining ongoing training, certifications and compliance with current regulations at MCW, CHW and the VA. Collaborates with Principal investigator, IRBs and sponsor in identifying and reporting of adverse events in a timely fashion per FDA guidelines Prepare IRB documents and reports using electronic systems. Experience with eBridge preferred. Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports. Process and ship lab specimens as necessary. IATA certification preferred. Phlebotomy experience preferred Develop and monitor study related budgets and provide reports as required to department administration and funding agencies. Work with CTO Managers in negotiating budgets with industry. Display familiarity in utilization of clinical trial management systems, proficiency with OnCore preferred. Participate in the... For full info follow application link. EEO/AA Minorities/Females/Vets/Disability The Medical College of Wisconsin is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, veteran status, disability or sexual orientation. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/208BF8FD3045411C Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.

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