Data Entry

• Coordinate the activities of clinical trials
• Manage and maintain study documentation and records
• Enter and review data in the trial’s electronic systems (eCRF)
• Manage and resolve queries
• Provide support during monitoring visits, audits and inspections
• Ensure compliance with applicable procedures and regulations
• Coordinate the dispatch and management of biological samples
• Collaborate with investigators, CRAs, sponsors and other professionals involved in the study

Explore Data Entry, Study Coordinator at Humaneva Group. Review requirements and application details.