This role will need to travel to Pittsburgh for training at the beginning of the employment.

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.

Independent study coordination including screening potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. Maintain accurate source documents related to all research procedures. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.