This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills. Responsibilities include EDC Entry and Query Resolution; developing strong working relationships and maintaining effective communication with study team members; developing strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office; assisting with the screening, recruiting, and enrollment of research subjects; performing patient/research participant scheduling; collecting patient/research participant history; coordinating follow-up care and laboratory procedures; adhering to an IRB-approved protocol; assisting in the informed consent process of research subjects; supporting the safety of research subjects; coordinating protocol-related research procedures, study visits, and follow-up care; complying with company and Sponsor policies, standard operating procedures (SOPs), and guidelines; scheduling subject visits and procedures. Qualifications include equivalent education and experience - High School Diploma and 1 years’ relevant work experience in clinical research; at least 1 year experience working in a clinical research setting preferred; working knowledge of clinical trials; working knowledge of the principles of Good Clinical Practices (GCP); in-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules; skill in carrying out required clinical procedures; working knowledge of medical terminology; ability to pay close attention to detail; ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients; applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies. This position is not eligible for sponsorship.