Clinical Research Coordinator

The Clinical Research Coordinator is responsible for the planning, coordination, and execution of clinical research studies, including the collection and management of clinical trial data. This role supports the conduct of safety and efficacy studies under the supervision of the Principal Investigator and in accordance with approved study protocols, company standard operating procedures, and current Good Clinical Practice guidelines. Supervisory Responsibilities: None

Responsibilities

Coordinate and support the planning, initiation, implementation, and day-to-day execution of clinical research studies in accordance with study protocols, sponsor requirements, SOPs, and current Good Clinical Practice guidelines; Prepare, organize, and maintain study materials and documentation, including informed consent forms, screening materials, source documents, and study logs; Explain study procedures to research participants, obtain informed consent, and confirm subject eligibility in collaboration with the Recruitment Department and study team; Prepare study areas, test materials, and supplies required for study conduct; Receive, log, weigh, prepare, and dispose of test articles in accordance with protocol and safety requirements; Conduct and coordinate daily clinical study activities to support efficient workflow and subject throughput; Monitor research subjects' responses, assign protocol-defined scoring, and accurately record adverse events and study data; Operate study-related instruments and equipment, ensuring proper data collection and documentation; Prepare, update, and maintain study data tables, subject databases, logs, and tracking tools; Collaborate with investigators, project managers, and internal departments to communicate study progress and support protocols and reports; Perform front-desk, participant-facing, and general administrative support activities; Maintain study files and administrative records in an inspection-ready condition; Order, stock, and maintain laboratory, clinic, and study supplies; Perform routine facility and study-area opening and closing procedures; Conduct cleaning, disposal, and housekeeping tasks related to study execution; Provide support to senior clinical research staff and management and perform other related duties as assigned

Requirements

Citizen or Permanent Resident of the country you are applying for, or hold or be able to obtain a valid working visa

Benefits

Programs and opportunities to develop new skills and build a diverse career; Safe, flexible and rewarding career