About the role
Company Description
Selva Infosys LLC operates at the intersection of medical practice compliance and automated workflow optimization, serving healthcare organizations that want to streamline operations. The company provides a complete financial lifecycle framework designed to reduce administrative friction and improve turnaround times for healthcare services. Its solutions help clinical and administrative teams ensure healthcare systems capture the full value of patient care while maintaining high compliance standards. Selva Infosys supports data-driven decision-making and efficient processes that benefit both providers and patients.
Role Description
The Senior Clinical Research Coordinator is a full-time, on-site role based in Manchester, NJ, responsible for leading and managing daily clinical research activities. This position oversees study start-up, coordinates patient recruitment and screening, obtains and documents informed consent, and ensures adherence to study protocols and regulatory requirements. The coordinator manages visit schedules, collects and verifies source data, maintains case report forms, and supports monitoring visits and audits. The role collaborates closely with investigators, research staff, and external partners to address operational issues, maintain high-quality documentation, and support timely completion of clinical trials. The Senior Clinical Research Coordinator also mentors junior coordinators, contributes to process improvement, and helps align research operations with institutional compliance and financial workflows.