Clinical Research Coordinator

Role DescriptionThis is a full-time Clinical Research Coordinator. The Clinical Research Coordinator will be responsible for overseeing and managing clinical research studies, coordinating recruitment and enrollment of study participants, executing informed consent processes, and managing study protocols. Additional tasks include ensuring compliance with applicable regulations, facilitating communication between study teams, maintaining research documentation, and providing support in the execution of high-quality clinical trials.QualificationsComprehensive knowledge and experience with Informed Consent processes and Protocol adherenceStrong background in Research and Clinical Research ExperienceProficiency with Clinical Trials processes and conducting them in compliance with guidelinesStrong organizational, communication, and attention-to-detail skillsAbility to work independently in a remote setting and manage multiple prioritiesKnowledge of Good Clinical Practice (GCP) guidelines and applicable regulatory requirementsExperience with electronic data capture (EDC) systems is a plusBachelor's degree in life sciences, healthcare, or a related field preferred