Clinical Research Coordinator III
Clinical Research Coordinator III
Med-Neurology - Pennsylvania-Pittsburgh - (26004892)
|
The University of Pittsburgh Department of Neurology seeks to hire a Clinical Research Coordinator. The coordinator will conduct all aspects of clinical research trials from site initiation through activation and completion under the direction of the Principal Investigator. Responsibilities include study start-up and documentation; budget development and fiscal tracking; IRB submissions and consent forms; protocol implementation across UPMC departments; participant recruitment, screening, enrollment, and follow-up; conducting study visits and neuropsychological assessments; obtaining medical histories, blood pressure screenings, and blood collection via phlebotomy as applicable; processing and shipping biological specimens; dispensing medications under physician or nurse practitioner orders; managing research supplies and equipment; and ensuring timely, accurate documentation and data entry. The coordinator will collaborate with investigators, research staff, IRB personnel, UPMC departments, sponsors, and monitors. Additional duties may include assisting with IRB protocols, the Research Registry, brain bank pager coverage, and community outreach activities. This position has a significant impact on program operations and may affect the health and well-being of research participants. The successful candidate must understand applicable policies and procedures, exercise independent judgment, and resolve unique problems through the collection and interpretation of information. A Master's degree is preferred.
|
Job Summary
Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.
Essential Functions
Oversees and prepares IRB applications.
Reviews/audits research studies; assists with next step determination.
Monitors study budgets and expenditures. Maintains and orders supplies as needed.
Assesses protocol feasibility; establishes protocol-specific recruitment plans.
Trains staff and oversees the work of student workers as directed.
Communicates effectively with study participants and potential community recruits. Identifies community education opportunities.
Facilitates research/project team meetings.
Resolves complex data collection issues.
Physical Effort
Must be able to get around a university setting. Can be sedentary for long period of times.
Assignment Category: Full-time regular
Job Classification: Staff.Clinical Research Coordinator III
Job Family: Research
Job Sub Family: Clinical Research
Campus: Pittsburgh
Minimum Education Level Required: Master's Degree
Minimum Years of Experience Required: 1
Will this position accept substitution in lieu of education or experience: Combination of education and relevant experience will be considered in lieu of education and/ or experience requirement.
Work Schedule: M-F, 8:30-5:00
Work Arrangement: On-Campus: Teams that work on campus, in an office, or in a lab.
Hiring Range: TBD Based Upon Qualifications
Relocation_Offered: No
Visa Sponsorship Provided: No
Background Check: For position finalists, employment with the University will require successful completion of a background check
Child Protection Clearances: Not Applicable
Required Documents: Resume, Cover Letter
Optional Documents: Not Applicable
Equal employment opportunity, including veterans and individuals with disabilities.
PI286350342