Clinical Research Coordinator I

Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Recruits research subjects and conducts interviews and research assessments.

• Overseeing the trouble-free running of clinical trials• Collecting data obtained from research, coding and analyzing it• Managing budgets set aside for research• Communicating with participants regarding study objectives• Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules• Liaising with laboratories regarding research findings• Monitoring the study to ensure that it complies with protocols, is ethically-conducted, and follows regulatory standards• Maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines• Directing the collection, labeling, storage and transport of all specimens• Making sure that all equipment and supplies needed for the study are in-stock and in good working order

Requires sitting, standing, walking, and lifting up to 50 lbs.

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.