CLINICAL RESEARCH COORD B/ C

Job description

Duties: Clinical Research Coordinator B: With minimal supervision, coordinate Phase II-IV clinical trials and registries. Recruit, consent and screen patients according to protocol. Schedule patient visits and any necessary testing. Monitor patients per protocol requirements and ensure adherence to protocol requirements. Organize and maintain all documentation required by the sponsor or CRO- includes source documentation, case report forms, and research charts. Prepare and submit IRB submissions from initiation to close-out. Collect, review and report study data, complete case report forms and resolve data queries, process and ship study specimens including blood, urine and tissue samples, Participate in initiation, monitoring, audit and close-out visits. Participate in study team meetings and ongoing protocol training/compliance meetings. Show vigilance in patient safety, protocol compliance and data quality. Adhere to all University of Pennsylvania, FDA and GCP guidelines.

Clinical Research Coordinator C: Independently manage Phase I-IV complex clinical trials, consent and screen patients according to protocol. Schedule patient visits and any necessary testing. Monitor patients per protocol requirements and ensure adherence to protocol requirements, Organize and maintain all documentation required by the sponsor or CRO - includes source documentation, case report forms, and research charts. Prepare and submit IRB submissions from initiation to close-out. Collect, review and report study data, complete case report forms and resolve data queries, process and ship study specimens including blood, urine and tissue samples. Participate in study team meetings and ongoing protocol training/compliance meetings. Assist in the development/maintenance of study specific case report forms and source document tools. Show vigilance in patient safety, protocol compliance and data quality. Adhere to all University of Pennsylvania, FDA and GCP guidelines.


Position is contingent on continued funding.

Qualifications: Clinical Research Coordinator B: Bachelor's degree and 2-4 years of related experience or equivalent combination of education and experience required.
Clinical Research Coordinator C: Bachelor's degree and 4-6 years of related experience or equivalent combination of education and experience required.

Both: Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations.

Reference Number: 40-24922

Salary Grade: 026/ 027

Employment Type: Exempt

Org: DM-Pulmonary, Allergy and Critical Care

Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.

Job Family: I-Technical/Professional Research

 

 

 

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Job No:
Posted: 2/8/2017
Application Due: 4/9/2017
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