Manager Data Management (Contract)

📋 Description

• Serve as the primary Data Management contact for assigned clinical studies, collaborating with
• Manage CROs and Data Management vendors, including priorities, project plans, scopes, timelines
• Act as a Data Management Subject Matter Expert from protocol review through database lock and study
• Develop and execute Data Management project plans covering timelines, milestones, quality control
• Oversee the quality and timeliness of vendor deliverables and ensure work meets established Data
• Monitor vendor performance, identify risks or issues, and escalate concerns to vendor management

🎯 Requirements

• Bachelor's or master's degree and 4–8+ years of experience in Clinical Data Management or a related
• Demonstrated experience managing CROs and Data Management vendors, preferably within global or
• Strong understanding of the drug development lifecycle and clinical data management processes.
• Knowledge of pharmaceutical industry guidelines, best practices, Good Clinical Practice (GCP), 21
• Familiarity with Electronic Data Capture (EDC) systems and general proficiency with Microsoft Word
• Knowledge of clinical data coding and related data management practices.

🎁 Benefits

• Contract position based in the United States.
• Hourly compensation of $50–$80.
• Opportunity to contribute to clinical and pharmaceutical trials across multiple development phases.
• Exposure to cross-functional collaboration spanning Clinical Operations, Medical, Biostatistics
• Opportunity to work on complex clinical programs within an oncology-focused environment.