Human Research Technologist - Urology
Listed on 2026-06-26
-
Research/Development
Clinical Research -
Healthcare
Clinical Research
Position Overview
The Human Research Technologist in Urology executes research protocols for sponsored clinical trials and investigator‑initiated research. This role supports research operations, including participant recruitment, data collection in clinical settings, medical record review, regulatory submissions and document management, and overall study coordination. The position will serve as the primary coordinator for assigned clinical trials and support additional studies in a backup or support role as needed.
Key Responsibilities- Recruitment:
Screen and recruit subjects for clinical trials; clearly describe study purpose, procedures, risks, benefits, and eligibility requirements; develop recruitment materials in collaboration with study teams. - Study visit management:
Schedule and coordinate study visits; collect study‑related data; maintain research databases and study files; communicate with participants throughout the study lifecycle; ensure adherence to protocols. - Data management:
Collect, enter, and maintain study data; support data quality control activities; contribute to the design and maintenance of data collection plans; report on study progress and findings to the research teams. - Regulatory submissions:
Develop, review, and submit Institutional Review Board (IRB) applications, continuing reviews, amendments, and reportable events in coordination with investigators and regulatory offices. - Research development support:
Work with study teams to draft new protocols, abstracts, and complete required forms for new research submissions; develop and design project materials including participant forms, questionnaires, reports, surveys, and other data collection instruments. - Study logistics:
Monitor and manage study logistics, including inventory, equipment, scheduling, and limited budget tracking as assigned. - Collaboration and communication:
Serve as liaison with Principal Investigators, physicians, study sponsors, study team members, and central research offices. - Scholarly contributions:
Contribute to manuscripts, journal publications, abstracts, and scholarly presentations as appropriate.
Bachelor's Degree, 3+ years of relevant experience; or an equivalent combination of education and experience accepted. Required
Certifications:
None.
The salary range for this position,including all possible grades, is $46,400.00 - $67,300.00.
Penn State provides a competitive benefits package for full‑time employees designed to support both personal and professional well‑being. In addition to comprehensive medical, dental, and vision coverage, employees enjoy robust retirement plans and substantial paid time off which includes holidays, vacation, and sick time. A generous 75% tuition discount is available to employees as well as eligible spouses and children.
Background ChecksEmployment with the University will require successful completion of background check(s) in accordance with University policies.
EEO StatementPenn State is an equal opportunity employer and is committed to providing employment opportunities to all qualified applicants without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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