#996 - Clinical Data Coordinator (CDC)

Responsibilities

• Cook up and manage clinical trial data collection, entry, and cleaning processes.
• Inspect case report forms (CRFs) for completeness, accuracy, and consistency.
• Spot, track down, and solve data discrepancies and queries promptly.
• Collaborate with clinical research associates (CRAs), investigators, and site staff to uphold data quality standards.
• Support the creation and upkeep of data management plans (DMPs), edit checks, and validation rules.
• Aid in database lock activities and final data reconciliation.
• Promote compliance with GCP (Good Clinical Practice), regulatory requirements, and internal SOPs.
• Keep accurate documentation and audit-ready records throughout the trial.

Requirements

• Advanced English level (B2/C1) for smooth team communication.
• Bachelor's degree in life sciences, health sciences, or a related field.
• 3+ years of experience in clinical data coordination.
• Hands-on experience with one or more EDC systems (e.g., Medidata Rave, Veeva Vault, Oracle InForm, or similar).
• Solid understanding of GCP guidelines and clinical trial processes.
• Strong attention to detail and data accuracy.
• Excellent organizational and time-management skills.
• Clear written and verbal communication skills, with the ability to collaborate across cross-functional teams.
• Experience with CDISC standards (SDTM, CDASH) is a plus.
• Experience working on multi-site and/or international studies is a plus.

Benefits

Competitive salary in USD.

100% Remote work.

Type of contract: Independent Contractor with Venon Solutions LLC.

Paid Time Off: 2 weeks / 10 business days.

Paid Holidays from the US calendar.

Working hours: Full-time EST, fully committed.