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Clinical Research Coordinator Iii

Company

The University of Pittsburgh
Address , Pittsburgh, Pa
Employment type FULL_TIME
Salary
Expires 2023-07-19
Posted at 11 months ago
Job Description

Clinical Research Coordinator III

Med-MIRM-Dr Chandan Sen Group - Pennsylvania-Pittsburgh - (23003931)
Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.

The University of Pittsburgh is committed to championing all aspects of diversity, equity, inclusion, and accessibility within our community. This commitment is a fundamental value of the University and is crucial in helping us advance our mission, which includes attracting and retaining diverse workforces. We will continue to create and maintain an environment that allows individuals to discover, belong, contribute, and grow, while honoring the experiences, perspectives, and unique identities of all.

The University of Pittsburgh is an Affirmative Action/Equal Opportunity Employer and values equality of opportunity, human dignity and diversity. EOE, including disability/vets.
The University of Pittsburgh requires all Pitt constituents (employees and students) on all campuses to be vaccinated against COVID-19 or have an approved exemption. Visit coronavirus.pitt.edu to learn more about this requirement.
Assignment Category Full-time regular
Job Classification Staff.Clinical Research Coordinator III
Job Family Research
Job Sub-Family Clinical Research
Campus Pittsburgh
Minimum Education Level Required Master's Degree
Minimum Years of Experience Required 1
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, 8:30 a.m. - 5:00 p.m.
Work Arrangement On-Campus: Teams that work on campus, in an office, or in a lab.
Hiring Range TBD Based Upon Qualifications
Relocation Offered Yes
Visa Sponsorship Provided Yes
Background Check For position finalists, employment with the University will require successful completion of a background check
Child Protection Clearances Not Applicable
Required Documents Resume
Optional Documents Not Applicable
Essential Functions Conducts and responsible for all study related activities including screening & consent and enrollments, data collection/entry, and compliance with regulatory process. Prepares strategies to improve enrollment/retention. • Performs literature reviews, and prepares manuscripts for publication; writes research papers and assists with writing complex papers. • Oversees and prepares IRB applications. • Reviews/audits research studies; assists with next step determination. • Monitors study budgets and expenditures. Maintains and orders supplies as needed. • Assesses protocol feasibility; establishes protocol-specific recruitment plans. • Trains staff and oversees the work of student workers as directed. • Communicates effectively with study participants and potential community recruits. Identifies community education opportunities. • Facilitates research/project team meetings. • Resolves complex data collection issues.
Physical Effort Requires sitting, standing, walking, and lifting up to 25 lbs.