The Pulmonary, Allergy, Critical Care and Sleep Medicine Division of the DOM is hiring for a Clinical Research Coordinator. The division is led by division chief Alison Morris, MD and Executive Administrator Barbara Suchonic. The division is made of up approximately 70 clinical staff and over 100 research staff who work in a variety of locations including: Bridgeside Point, Biomedical Science Tower (BST), UPMC Hospitals including Presbyterian, Shadyside, East, Jameson and Mercy. The division provides world class services across 10 inpatient services at five hospitals and over 70,000 outpatient office visits. We have a major research mission that focuses on basic, clinical, and translational research on the lung, microbiome, COVID-19, sleep medicine, and allergy and immunology.
The Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine is currently seeking a Clinical Research Coordinator (CRC) to join a nationally recognized research institution participating in several federally funded and industry sponsored research studies. The Clinical Research Coordinator will directly report to the Director of the Center for Sleep and Cardiovascular Outcomes Research and work closely with principal investigators, study staff, and clinical staff to support the activities of the Center. This position will be involved in all aspects of coordinating research projects.
A successful candidate will: Assist with and adhere to Institutional Review Board (IRB) renewal, modification, and approved protocols. Conduct hands-on subject recruitment. Screen subjects to determine eligibility. Schedule and complete study visits and follow-up appointments. Assist with training staff. Maintain accurate source documentation. Correct issues with data collection.
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.
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.
Developing and enacting recruitment plan for sleep-related research studies.Coordinating protocol-related research procedures, study visits, and follow-up appointments.Completing and overseeing data entry and data management.Building a strong rapport with potential and enrolled subjects through frequent telephone/text contact.