Clinical Research Specialist

The Clinical Research Specialist will work closely with the Principal Investigator to facilitate and coordinate daily activities for clinical trials, including study testing, enrollment, and longitudinal cohort studies. This role involves ensuring site compliance with research protocols, maintaining IRB documentation, and providing accurate data collection and reporting to sponsors and study databases. The specialist will also monitor patient eligibility, assist with the informed consent process, and collaborate with internal and external research teams to maintain study quality and integrity.