Clinical Research Coordinator

Benefits

Qualifications

• •2–3+ years of Clinical Research Coordinator (CRC) experience
• •Strong knowledge of ICH-GCP, FDA regulations, and clinical trial operations
• •Experience with patient recruitment, screening, and consent
• •Experience with EDC systems and source documentation
• •Ability to manage multiple studies and deadlines independently
• •Strong communication and organizational skills
• •Exposure to complex clinical trials and advanced protocols
• •4 more items(s)

Responsibilities

• •This role is ideal for candidates with prior CRC experience who are comfortable working directly with sponsors, managing patients, and ensuring full protocol and regulatory compliance
• •Serve as primary coordinator for assigned clinical trials
• •Manage study startup, maintenance, and closeout activities
• •Coordinate patient visits, scheduling, and follow-ups
• •Conduct patient screening, recruitment, and enrollment
• •Perform clinical procedures and patient assessments per protocol
• •Maintain accurate source documentation and EDC data entry
• •Ensure ICH-GCP compliance and protocol adherence
• •Communicate with sponsors, CROs, and monitors
• •Prepare for and support monitoring visits, audits, and inspections
• •Resolve data queries, deviations, and study-related issues
• •Collaborate with the Principal Investigator (PI) on eligibility, safety, and oversight
• •9 more items(s)