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Job Description & How to Apply Below
As a key player in the team, you will report directly to senior management while independently guiding projects.
Your role will require close collaboration with Data Management, Statistics, IT, and Quality Control departments to design and develop eCRFs and manage studies through effective clinical data management systems. A strong background in compliance with industry regulations is essential.
Key Responsibilities:
• Spearhead eCRF design and setup for clinical trials
• Direct study management adhering to international standards
• Optimize database processes to support team efficiency
• Maintain compliance with ICH guidelines and local regulations
• Engage with cross-functional teams for enhanced project delivery
Requirements:
• Bachelor’s degree or equivalent work experience
• Minimum 5-7 years in clinical data management
• Experience leading eCRF development projects
• Proven track record with CDMS like Medidata Rave
• In-depth knowledge of clinical compliance regulations
Bring your expertise to Veristat and influence effective clinical research through your programming skills.
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Position Requirements
10+ Years
work experience
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