Clinical Research Coordinator II

University of Pittsburgh; Pittsburgh (Allegheny County); Presencial; USD 60.000 - 75.000; Jornada completa

Descripción de la vacante

The University of Pittsburgh in Pittsburgh is seeking a Clinical Research Coordinator II to conduct assessments and ensure protocol adherence across studies conducted in the Med-Medicine division.

The role involves coordinating visits, obtaining testing, managing data in RedCap/Qualtrics, and serving as a liaison among investigators, staff, and external partners. A Bachelor's degree and 2 years of relevant experience are required, with on-site work schedule Monday-Friday.

Formación

• Bachelor's degree required for consideration.
• Minimum 2 years of research or clinical coordination experience.
• Experience with IRB processes and study protocol adherence.
• Ability to manage data using regulatory and database systems.

Responsabilidades

• Coordinate eligibility, visits, education and required testing.
• Perform fibroscans, EKGs, phlebotomy and sample processing.
• Mentor new staff and support the PI on studies.
• Manage inventory and ordering of study materials.
• Serve as liaison between subjects, investigators, outside providers and sponsors.
• Submit data to databases and assist with IRB submissions.
• Maintain study charts and source documentation.
• Ensure proper sample collection, storage and shipment to labs.

Conocimientos

BIA measurements

Dynamometer calculations

Fibroscan testing

Data entry

RedCap

Qualtrics

Communication with PI

Educación

Bachelor's Degree

Herramientas

RedCap

Qualtrics

Descripción del empleo

Job Description - Clinical Research Coordinator II (26006811)

Clinical Research Coordinator II

Med-Medicine - Pennsylvania-Pittsburgh - ( 26006811 )

Job Summary

Conducts research assessments on study participants. Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data collection.

Essential Functions

Coordinate activities for study protocols including subject eligibility, appointments, subject education, preparation for study visits; completes subject visit requirements including required testing from eligibility through follow up. Protocols require staff be able to perform BIA measurements, dynamometer calculations, fibroscan testing, and other research testing. Maintains ongoing communication with investigator in a timely manner for all protocol follow up. Completes and submits data as required for study protocols; works with PI to establish databases as needed. Utilize RedCap, Qualtrics, as well as additional databases as required by protocols. Maintains subject research chart with all required source documentation. Act as a liaison between subject, investigator, outside providers, any ancillary departments, as well as any sponsoring agency or organization. Maintains study inventory to confirm adequate supply of materials within budget requirements. This includes ordering supplies and preparing study kits. Obtain biological research samples as required from subjects. Ensure proper preparation and processing of samples. Delivering them to ancillary laboratories as necessary or maintaining proper storage of samples. Shipping to central laboratories as appropriate. Maintain ongoing IATA certification. Other duties as assigned.

• 1. Conduct complex research assessments on study participants - including obtaining fibroscans; performing EKGs; phlebotomy, sample processing;
• 2. Mentors new staff;
• 3. Consents research participants to observational studies;
• 4. Maintains inventory of lab supplies and orders as needed;
• 5. Continue as main contact as the coordinating site to external sites for collaborative studies initiated through or PI
• 6. Works with PI to submit new studies as well as modifications and renewals to the IRB;
• 7. Completes and corrects data entry on multiple projects utilizing multiple databases;
• 8. Meets with external staff for sponsored studies

Physical Effort

Must have ability to navigate around UPMC facilities and Pitt campus with and without research equipment; dexterity and fine motor skills to perform research testing using multiple types of equipment; ability to work with multiple computer programs for electronic database entries and other computer tasks; must be able to perform modest lifting. Ability to stand for long periods of time for specimen processing and other research tasks.

The University of Pittsburgh is an equal opportunity employer / disability / veteran.

Assignment Category Full-time regular

Job Classification Staff.Clinical Research Coordinator II

Job Family Research

Job Sub-Family Clinical Research

Campus Pittsburgh

Minimum Education Level Required Bachelor's Degree

Minimum Years of Experience Required 2

Will this position accept substitution in lieu of education or experience? Combination of education and relevant experience will be considered in lieu of education and/ or experience requirement.

Work Schedule Monday-Friday 8am-4:30 pm

Work Arrangement On-Campus: Teams that work on campus, in an office, or in a lab.

Hiring Range TBD Based Upon Qualifications

Relocation Offered No

Visa Sponsorship Provided No

Background Check For position finalists, employment with the University will require successful completion of a background check

Child Protection Clearances Not Applicable

The University of Pittsburgh is an equal opportunity employer / disability / veteran.