Clinical Research Coordinator

Come join our client, a rapidly growing life sciences digital technology company, as they embark upon an exciting new solution in the clinical trials space. Our client supports high-quality clinical studies, and the team helps connect patients with emerging therapies and innovative care pathways.They seek an experienced bilingual (Spanish/English) Clinical Research Coordinator to play a central role in coordinating and managing clinical trial activities at the site level, ensuring studies are executed efficiently, ethically, and in accordance with regulatory standards.This position is office-based in New York City, with one WFH day per week.Qualifications of the Clinical Research Coordinator:Bachelor’s degree in life sciences, healthcare, or a related field preferred.Minimum of two years’ experience in clinical research coordination, monitoring, or site operations.Working knowledge of clinical research regulations and compliance standards.Strong organizational, analytical, and problem-solving abilities.Ability to collaborate effectively with cross-functional teams and external partners.Strong time-management and prioritization capabilities.Demonstrated commitment to high-quality research execution.Professional approach to sponsor and partner engagement.Experience in early-stage or growing research environments is a plus.Bilingual in English/Spanish. Responsibilities of the Clinical Research Coordinator:Partner with internal leadership and investigators to evaluate potential study participation.Assist sponsors and research partners with feasibility reviews and site evaluations.Compile, review, and submit required regulatory and administrative documentation.Prepare and manage ethics committee and IRB submissions and approvals.Organize and maintain regulatory records in electronic filing systems following GCP standards.Support participant identification, screening, and informed consent processes when authorized.Coordinate and conduct protocol-required visits and procedures.Maintain accurate source documentation and electronic data entries.Monitor participant safety and report safety events per study guidelines.Work closely with investigators and site staff to ensure protocol adherence.Maintain enrollment, deviation, and tracking logs.Prepare documentation and materials for study close-out activities.Perform additional duties related to clinical trial operations as needed.Occupational Code: Clinical Research Coordinator (CRC) 11-9121.01