Note: The job is a remote job and is open to candidates in USA. United Consulting Hub is seeking a detail-oriented Clinical Research Coordinator to support the planning, coordination, and execution of clinical research studies and clinical trials. The role coordinates study operations, supports sites and patients, maintains clinical documentation and data, and ensures compliance with protocols, ICH-GCP guidelines, regulations, and company SOPs.
Responsibilities
- Support the day-to-day coordination and execution of clinical research studies and clinical trials
- Assist with study start-up activities, site activation, site initiation, and ongoing study operations
- Coordinate study activities, timelines, deliverables, and follow-up actions across assigned clinical studies
- Maintain essential documents, study files, trackers, correspondence, and clinical trial records
- Support patient recruitment, pre-screening, screening, scheduling, follow-up, and study visit activities
- Enter, review, reconcile, and maintain accurate clinical data within EDC, CTMS , and other clinical systems
- Assist with monitoring visits, quality reviews, audits, regulatory inspections, and study-related reporting activities
- Identify, document, track, and escalate protocol deviations, data discrepancies, compliance issues, and operational risks
- Ensure study activities are performed in accordance with ICH-GCP, FDA regulations, SOPs, informed consent requirements, and approved study protocols
- Collaborate with Clinical Operations, Data Management, Pharmacovigilance/Safety, Quality, Regulatory, and other cross-functional teams
- Participate in study meetings, prepare meeting documentation, and follow up on assigned action items, deliverables, and timelines
- Maintain effective communication with study teams and relevant stakeholders in a remote and cross-functional environment
- Escalate study-related risks, compliance concerns, data quality issues, and operational challenges to appropriate team members
- Perform additional clinical research, study coordination, documentation, and administrative activities as assigned
Skills
- Experience: 0–2 Years
- • Basic understanding of clinical research processes, clinical trial documentation, study protocols, informed consent, and essential study records
- • Familiarity with clinical trial systems such as EDC, CTMS, eTMF , or similar clinical research platforms
- • Proficiency in Microsoft Office , including Word, Excel, PowerPoint, and Outlook
- • Strong attention to detail with the ability to maintain accurate, complete, and timely documentation
- • Good written and verbal communication skills with the ability to collaborate effectively with cross-functional teams
- • Strong organizational and time-management skills with the ability to manage multiple study activities and competing priorities
Benefits
- Remote work
Company Overview