Join Pharma Medica Research as a Clinical Data Coordinator and ensure high-quality clinical research. This role emphasizes data entry, eCRF usability, and lab data management in a collaborative environment.

As a key member of our data management team, you will handle User Acceptance Testing (UAT) for electronic Case Report Forms. Your responsibilities include entering data accurately, coding medical history using MedDRA, and managing laboratory data within strict timelines. Contribute actively to resolving data queries and collaborating with clinical staff and sponsor monitors for effective study execution.

Key Responsibilities:
• Perform User Acceptance Testing on eCRFs
• Accurately enter data from clinic documents
• Code medical history and medications in EDC
• Manage laboratory data and requisition tracking
• Generate and review tables for Clinical Study Reports

Requirements:
• Diploma in scientific or health...