Clinical Research Coordinator II

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.

This coordinator will do all Coordinating functions (screening patients, reviewing consent, obtaining data for study, working in databases, collecting research documents as required by protocols, working with patients and families on floors, data collection). This position would require the individual to understand IT and how to manage different interfaces.

Need to have a good understanding on clinical process and pathways. Will also be responsible for interfacing, data collection and statistical outcomes.

Must be able to sit or stand for prolonged periods of time

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.