Manager Clinical Research occupation at Medical College of Wisconsin in Milwaukee

Medical College of Wisconsin is currently interviewing Manager Clinical Research on Tue, 21 Aug 2012 03:27:56 GMT. POSITION PURPOSE Manage research activities of assigned sections as directed by the Pediatric Cancer Clinical Trial Director. Duties will include coordination of overall clinical research within the section to ensure smooth operation of clinical trials. Provide leadership and oversight to research teams and facilitate the achievement of program goals. Recruit, train, and supervise clinical...

Manager Clinical Research

Location: Milwaukee Wisconsin

Description: Medical College of Wisconsin is currently interviewing Manager Clinical Research right now, this occupation will be placed in Wisconsin. Further informations about this occupation opportunity kindly see the descriptions. POSITION PURPOSE

Manage research activities of assigned sections as directed by the Pediatric Cancer Clinical Trial Director. Duties will include coordination of overall clinical research within the section to ensure smooth operation of clinical trials. Provide leadership and oversight to research teams and facilitate the achievement of program goals. Recruit, train, and supervise clinical research staff.

ESSENTIAL DUTIES

1. Act as a resource for investigators and support staff. Facilitate preparation and management of faculty research projects. Provide oversight for preparing IRB protocols and compiling budget and supporting application materials. Management of clinical trial activities includes budget preparation and tracking, and reporting to funding agencies as required to ensure the success of additional resource requests.

2. Advise investigators and support staff on administrative and regulatory aspects of human subject research.

3. Provide leadership for Clinical Research Coordinators, Clinical Research Assistants, Research Nurses. Monitor for consistent adherence to research guidelines, assisting with problem solving and training in research principles as needed. Provide research leadership and education for the section. Act as the main section resource relating to current human research regulatory requirements.

4. Develop and implement policies, procedures and organizational tools to ensure compliance with MCW, state and federal standards.

5. Manage data systems supporting research activities. Correspond with IRBs as needed.

6. Assist in the development and management of budgets.

7. Act as a liaison between the Pediatric Cancer Clinical Trial Director and research staff. Work closely with other departments and external agencies to advance the department’s research goals.

8. Develop, implement and monitor research QI activities. Implement and conduct quality control processes to ensure the highest data and research standards.

9. Utilize quality improvement tools to facilitate improvement of systems & processes.

10. Contribute to manuscript and abstract preparation, as well as preparation of posters and other materials for presentation of research findings.

11. Oversee recruitment, screening, enrollment and proper consenting for program participants.

12. Report program data and progress to study investigators. Work with Principle Investigators to develop, implement, and maintain comprehensive databases and files related to the program.

13. Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators.

14. Assure compliance with all relevant IRB and other regulatory agency requirements.

15. Maintain program timeline including tracking deadlines for program components.

16. Oversee program outreach activities including acting as a liaison with community organizations.

17. Develop infrastructure to monitor study related budgets and funding streams. Provide reports as required to investigators and department administration.

18. Coordinate recruitment and training of clinical research staff.

Qualifications

MINIMUM POSITION QUALIFICATIONS

Appropriate education and/or experience may be substituted on equivalent basis

Education: Bachelor’s Degree in a relevant field.

Experience: 6 years of experience in research program coordination. Experience with program management in a medical research or educational environment preferred. Prior work with clinical research or patient care preferred.

Certifications/Licenses: CCRC or CCRP preferred. CITI training required within 90 days of hire.

KNOWLEDGE, SKILLS, & ABILITIES

Excellent oral and written communication skills are essential. Strong critical thinking, problem solving and attentiveness to detail required. Strong computer skills. Sufficient knowledge of program study area.
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This occupation starts available on: Tue, 21 Aug 2012 03:27:56 GMT

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