Mary Hetrick

Mary Hetrick has over 25 years of experience in clinical research, currently serving as a Human Protection Specialist at Celerion since June 1998, where responsibilities include reviewing client protocols, writing informed consent forms, and submitting documents to the IRB. Previously, as a Clinical Conduct Specialist at Celerion, Mary collaborated with the Clinical Study Manager and Clinical Conduct Associates to implement studies and manage necessary logistics and documentation. Prior to Celerion, Mary worked as a Clinical Conduct Associate at Harris Laboratories from June 1995 to June 1998, where duties encompassed conducting vital signs, phlebotomy, ECGs, and ensuring data quality during study procedures.