Life Sciences Data Management Consultant
hace 2 días
Veeva Systems is a pioneering industry cloud company, dedicated to helping life sciences organizations bring therapies to patients faster. With a strong commitment to customer success, employee success, and speed, we've achieved significant growth in recent years, surpassing $2 billion in revenue.
The RoleAs a key member of our CDMS Professional Services team, you'll be responsible for working with customers to understand their data management needs and challenges, providing guidance and direction to ensure clinical trials are designed effectively. Your expertise in EDC software configuration will be crucial in implementing study designs that adhere to Good Clinical Data Management Practices and Veeva standards.
Responsibilities- Review and understand clinical protocol requirements
- Prepare, review, and finalize project specifications applying industry and Veeva best practices
- Configure forms, rules, and other study items with Veeva Vault CDMS product during development
- Support developers and testers during the project lifecycle
- Conduct on-site or remote user acceptance testing with the customer
- Ensure a smooth transition of the study to the customer
To succeed in this role, you'll need:
- 2+ years' experience in end-to-end data management-related activities
- Direct experience working with EDC clinical software solutions in clinical operations and/or trial management
- Life sciences industry experience and knowledge of clinical trial process preferred
We offer a competitive salary, ranging from $85,000 to $115,000 per annum, depending on experience. Additionally, you'll enjoy:
- Allocations for continuous learning & development
- Health & wellness programs
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