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UPMC is seeking a technical OnCore CTMS specialist to coordinate intake and initial setup for clinical research studies. You will build protocol shells, calendars, and budgets in OnCore, conduct QC checks, and train staff to support calendar builds.
The role requires 3+ years of hands-on experience with OnCore and the ability to manage multiple timelines while collaborating with study teams and external vendors. In-office presence is required three days per week.
Under the direction of the Senior OnCore Administrator, this technical position is responsible for coordinating the intake and initial setup of clinical research studies within the OnCore Clinical Trials Management System (CTMS). It plays a critical role in supporting clinical research operations by managing the protocol build process. This position serves as a liaison between study teams and external vendors, ensuring timely and accurate setup of protocol shells, study calendars, and budgets. The specialist is responsible for initiating builds, maintaining task lists, implementing quality control processes to ensure data integrity and compliance, and training staff.
Please note that this position is in-office three days per week.
Must be legally authorized to work in the United States, without requiring, now or in the future, sponsorship for employment visa status. UPMC does not offer any type of sponsorship (H-1B, permanent residence, etc.) UPMC does not participate in STEM OPT.
UPMC is an Equal Opportunity Employer/Disability/Veteran