University of Pittsburgh · 8 hours ago
Clinical Research Coordinator - PMR
Pittsburgh, PA
Full-time
Onsite
New Grad, Entry Level
$17.74/hr - $22.17/hr
0+ years expThe University of Pittsburgh is seeking a qualified Clinical Research Coordinator in the Department of Physical Medicine & Rehabilitation. This role involves assisting with clinical trials, recruiting research subjects, and ensuring compliance with study protocols under the guidance of the Clinical Trials Manager and Principal Investigator.
Higher Education
No H1B
Responsibilities
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols
Recruits research subjects and conducts interviews and research assessments
Coordinate site initiation documentation and activities
Recruit and consent study patients
Handle the fiscal review process and assist with developing clinical trial budgets
Monitor compliance with study protocol
Coordinate protocol driven procedures and assessments across clinical departments within UPMC at appropriate time intervals
Generate compliant source documents and be responsible for timely completion of case report forms for all study visits and documentation and proper reporting for adverse events
Assist with other departmental duties, including helping with other IRB protocols and registry recruitment as requested
Biosample collection, processing, and storage of samples in biorepository
Participant recruitment and consent
Effective communication with clinicians and other health professionals
Data and compliance tracking
Patient retention
Accurate reporting
Qualification
Required
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols
Recruits research subjects and conducts interviews and research assessments
Coordinate site initiation documentation and activities
Recruit and consent study patients
Handle the fiscal review process and assist with developing clinical trial budgets
Monitor compliance with study protocol
Coordinate protocol driven procedures and assessments across clinical departments within UPMC at appropriate time intervals
Generate compliant source documents
Responsible for timely completion of case report forms for all study visits and documentation
Proper reporting for adverse events
Assist with other departmental duties, including helping with other IRB protocols and registry recruitment as requested
Biosample collection, processing, and storage of samples in biorepository
Participant recruitment and consent
Effective communication with clinicians and other health professionals
Data and compliance tracking
Patient retention
Accurate reporting
Bachelor's Degree
No experience required
Combination of education and relevant experience will be considered in lieu of education and/or experience requirement
Availability to contact patients or providers at various times and in various settings
Ability to travel to multiple sites and between buildings on campus
Resume, Cover Letter
Preferred
A professional degree in the health field with prior research experience
Phlebotomy training preferred
Candidates who do not already have documented phlebotomy training will be required to receive training upon hiring
Company
University of Pittsburgh
The University of Pittsburgh is a top-ranked, public institution in Pennsylvania and a member of the Association of American Universities of leading research universities.
10001+ employees
Funding
Current Stage
Late StageLeadership Team
Alexandra Costlow
Communications Specialist for the CFO / SVC Office
Narahari Sastry
Senior Vice Chancellor & CFO
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