Data Review & Validation:
Review clinical trial data or research data for completeness and accuracy.
Identify and correct discrepancies in data entries.
Data Quality Assurance:
Ensure compliance with protocols, SOPs, and regulatory standards.
Conduct quality checks and generate queries for data inconsistencies.
Documentation & Reporting:
Maintain accurate records of data changes, discrepancies, and resolutions.
Prepare reports and summaries for clinical trial teams or project managers.
Collaboration with Teams:
Work closely with clinical operations, data management, and biostatistics teams.
Support project teams in resolving data-related issues.
Regulatory Compliance:
Ensure that all data handling meets regulatory and ethical standards (e.g., ICH-GCP guidelines).
Health insurance for employees and dependents
Provident Fund (PF) and retirement benefits
Paid leave and holidays
Performance bonuses or incentives
Training and certification opportunities (e.g., CDISC, GCP)
Flexible work arrangements or hybrid options
🔬 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