Clinical Research Coordinator - Night Shift (MBBS Required)

About the role

A Clinical Research Coordinator is sought to support and coordinate clinical research activities across ongoing and upcoming clinical trials. The role covers patient screening and recruitment, study feasibility, documentation, data management, protocol and regulatory compliance, and coordination of remote clinical research operations. It is open to night-shift work and requires an MBBS degree.

Key responsibilities

• Screen patients by reviewing medical records, running pre-screening and outbound calls, and documenting screening outcomes; recruit and enroll participants with investigators and study teams.
• Coordinate day-to-day trial activities according to approved protocols, track timelines and deliverables, and liaise with sites, investigators, sponsors and CROs.
• Support feasibility questionnaires, site capability assessments and study start-up.
• Help collect and maintain clinical data, support CRFs and EDC systems, and resolve queries.
• Ensure activities follow study protocols and GCP, escalate deviations and support corrective and preventive actions.
• Prepare documentation for IRB/Ethics Committee submissions, regulatory files, monitoring visits and audits.
• Provide remote support, prepare status reports and escalate delays or risks.
• Guide study coordinators and research staff, share medical knowledge and help update training materials.

Required profile

• MBBS degree.
• Understanding of clinical research principles, patient care and clinical terminology.
• Knowledge of GCP and clinical trial processes.
• Excellent written and verbal English, with strong telephone communication and patient interaction skills.
• Strong analytical, organizational and documentation skills; able to work independently in a remote or offshore environment.
• Prior experience in clinical research, trials, medical research, patient recruitment or a related field is preferred but not mandatory.

Required skills

• Microsoft Office, especially Excel, Word and PowerPoint.
• Preferred: familiarity with EDC systems, patient chart review, telephone screening, regulatory and ethics documentation, IRB/Ethics submission processes, and clinical trial terminology (CRFs, informed consent).

What we offer

• Flexible working environment.
• Opportunity to work with international clinical research teams and exposure to global trial practices.
• Professional development and learning opportunities.