Assumes day-to-day responsibilities for staff in research study administration, recruitment, and logistics. Develops and implements staff operational plans/systems for recruitment, data collection, and associated research oversight tasks to meet project goals and deliverables. Oversees patient recruitment and enrollment, including trains staff on enrollment guidelines, regulations, and standard operation procedure. Customizes standard practices and clinic flow to meet study protocols and participants. Designs and implements system for organizing data collection forms and procedures, including developing study protocols, designing study forms, collaborating to set up database systems, developing data monitoring procedures, and supervising data entry and maintenance of raw data. Develops and ensures quality control procedures, including reviewing data for accuracy and completeness. Ensures adherence to protocols related to ICH-GCP. Leads the work of others, but does not have direct management responsibility for staff, students, or temps.
Manages day-to-day Program responsibilities for staff in research study administration, recruitment, and logistics. Develops and implements operational plans and systems for recruitment, data collection, and meeting project goals and deliverables. Ensures study protocols and quality control procedures are met.
The Clinical Research Support Office, within the Senior Vice Chancellor of Health Science, is seeking a Clinical Research Coordinator Manager. The individual in this role will Manages day-to-day Program responsibilities for staff in research study administration, recruitment, and logistics. Develops and implements operational plans and systems for recruitment, data collection, and meeting project goals and deliverables. Ensures study protocols and quality control procedures are met. Will be required to communicate effectively with study participants and the study team. The job duties outlined above include common job responsibilities for this title and job level. This position will require travel from in and around Pitt and UPMC campuses. The University reserves the right to assign additional duties not listed here.Manages day-to-day Program responsibilities for staff in research study administration, recruitment, and logistics. Develops and implements operational plans and systems for recruitment, data collection, and meeting project goals and deliverables. Ensures study protocols and quality control procedures are met.
Sitting and standing for long periods. Reading small print. Walking around campus. Bending and lifting up to 10 pounds. Pull cart with study materials. Carry study material. Work in office for full day.
The University of Pittsburgh is an equal opportunity employer / disability / veteran.
Job Details
- Assignment Category: Full-time regular
- Job Classification: Staff.Clinical Research Coordinator Manager
- Job Family: Research
- Job Sub-Family: Clinical Research
- Campus: Pittsburgh
- Minimum Education Level Required: Bachelor's Degree
- Minimum Years of Experience Required: 3
- 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: Monday - Friday, 8:30 a.m. - 5:00 p.m
- 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