Research Protocols
ClinicalResearchCoordinator1(A)FullTime
“Clinical Research Coordinator 1 (A) Full Time at Research Protocols. Skills: Data management, Clinical research protocols, Patient coordination. Perform chart review/pre-screening. Coordinate simple clinical research protocols”
Industry & Context.
Problem solves when operational failures occur; Helps problem solve protocol deviations; Helps problem solve unanticipated occurrences
Flexibility to travel to all BPEI sites as needed, Ability to work evenings, nights, and weekends as necessary
What They're Looking For.
Must Have
Bachelor’s degree, 1 year of relevant experience, Skill in completing assignments accurately, Ability to analyze, organize and prioritize work, Ability to process and handle confidential information, Ability to work evenings, nights, and weekends, Commitment to the University’s core values, Ability to work independently, Ability to work in a collaborative environment
Nice to Have
Flexibility to travel to all BPEI sites, Ability to handle multiple clinical trials, Serve as back up coordinator
What You'll Do.
Perform chart review/pre-screening
Coordinate simple clinical research protocols
Maintain enrollment procedures
Coordinate routine clinical studies activities
Perform research tests/experiments
Adapt procedures for quality improvement
Operate clinical research equipment
Problem solve operational failures
Observe and inform PI/supervisor of adverse events
Address adverse events per protocol
Advocate for study participants
Identify protocol deviations
Report protocol deviations
Problem solve unanticipated occurrences
Follow fundamental requirements of regulatory bodies
Maintain study-specific regulatory binders
Maintain requisite skills and training
Adhere to University policies
Safeguard University assets
Establish patient/participant screening procedures
Obtain relevant medical information
Handle multiple clinical trials
Serve as back up coordinator
Complete corrections/queries at audits
Take action to correct deviations
Establish/maintain contact with patient/participants
Establish/maintain contact with health care providers
Establish/maintain contact with community agencies
Establish/maintain contact with study sponsors
Update agencies regarding research project status
Provide in-service education to staff
Provide in-service education to patients/participants
Prepare annual reviews for IRB
Submit annual reviews to IRB
Maintain consent forms
Maintain sponsor correspondences
Notify IRB of protocol amendments
Notify IRB of safety reports
Notify IRB of serious adverse events
Implement research protocol
Monitor participant adherence to protocol
How You'll Work.
Team & Collaboration
Ability to work in a collaborative environment
Process & Methodology
Planning study timelines, Planning study schedules
Applying for this Clinical Research Coordinator 1 (A) Full Time role?
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