Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR

JOB PURPOSE

The Clinical Research Coordinator will coordinate and manage all aspects of clinical research studies, ensuring

compliance with protocols, regulatory requirements, and ethical standards. This role involves recruiting and screening

potential study participants, collaborating with healthcare professionals, monitoring adverse events, and maintaining

meticulous documentation. Fluency in Spanish is preferred for this position.

ESSENTIAL JOB FUNCTIONS

• Study Coordination : Coordinate and manage all aspects of clinical research studies, ensuring compliance with

protocols, regulatory requirements, and ethical standards.

obtaining informed consent, and ensuring eligibility criteria are met.

conducted in accordance with protocol, Good Clinical Practice (GCP), and applicable regulations.

professionals involved in the study. Communicate regularly to address issues and ensure the smooth progress

of the research.

regulatory authorities, sponsors, and other relevant stakeholders.

report forms, source documents, and other study-related records.

compliance with regulatory standards.

stakeholders. Provide regular updates on study progress and address inquiries.

working proactively to prevent potential problems. Please be advised that job duties and locations may change based on the needs of the Company

QUALIFICATIONS AND EXPERIENCE

position.

WORKING CONDITIONS AND PHYSICAL REQUIREMENTS

professionals, and study participants.

DIRECT REPORTS

This position does not have any direct reports but will work closely with study team members, including research

assistants, data coordinators, and other staff involved in the study.