Senior Consultant - Clinical Data Programming

📋 Description

• Act as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to
• Work with customers to interpret clinical protocol requirements and project specifications
• Lead database development activities per the project plan, coordinating with sponsor, CRO, and
• Coordinate with clinical data providers (central labs, ECG, eCOA, IRT, etc.) to configure data
• Configure forms, rules, and other study items in Vault CDMS, and build custom SQL-based listings
• Run on-site or remote user acceptance testing, managing feedback, issue resolution, and study

🎯 Requirements

• 5+ years of experience with EDC clinical software, covering end-to-end data management (database
• Solid understanding of clinical trial processes, particularly around data collection and review
• Programming experience in languages such as SAS, R, JSON, Python, or SQL, with the ability to pick
• Background in the life sciences industry (pharma, biotech, medical device, CRO, or academic/public
• Experience in a customer-facing role, ideally within software professional services or consulting
• Ability to work independently and collaboratively in a fast-paced, dynamic environment while

🎁 Benefits

• Private health insurance
• Flexible paid time off plus local public holidays
• Pension / retirement plan contributions
• 1% charitable giving program