Review and code adverse events (AEs), concomitant medications, and medical histories according to standardized dictionaries.
Ensure accuracy, completeness, and consistency of clinical trial data.
Collaborate with Clinical Data Management teams, biostatisticians, and clinical operations.
Resolve coding queries or discrepancies in the trial database.
Support database locks, analysis, and regulatory submissions.
Follow Good Clinical Practice (GCP) guidelines and regulatory compliance standards.
Competitive base salary with performance-based bonuses.
Provident Fund (PF) contributions and Gratuity benefits.
Health insurance covering employee and dependents.
Life and accidental insurance coverage.
Comprehensive medical, dental, and vision insurance in multinational organizations.
Access to Employee Assistance Programs (EAPs) for mental health support.
Wellness initiatives such as annual health check-ups or gym reimbursements.
Paid time off (PTO) — annual leave, casual leave, and sick leave.
Public holidays and optional holidays.
Flexible working hours and hybrid/remote work options depending on company policy.
Maternity and paternity leave as per statutory and company guidelines.
Training in clinical coding standards, MedDRA/WHO-DD/ICD dictionaries, and regulatory compliance.
Opportunities to advance to:
Senior Clinical Data Coder
Clinical Data Management Specialist
Data Manager / Clinical Operations Manager
Support for certifications in clinical research, pharmacovigilance, or clinical data management.
🔬 Services & Capabilities Medpace offers a full-service model encompassing all phases of clinical trials (Phase I-IV), providing services such as: Study Start-up and Clinical Trial Management Clinical Monitoring and Data Management... Read More