Clinical Data Programmer
About the role
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- Collaborates with Project Team to agree on vendor expectations for the collection and transfer of data.
- Responsible for configuring the data loading tools based on data collection specifications.
- Represents Data Management at UAT handover meetings.
- Performs creation of outbound data deliveries, verification of file format, and reports errors to Project Data Lead.
- Performs verification of inbound data file formats and content and loading of data for the blinded presentation to the reviewer
- Installation of eCRF databases and preparation of databases for review sessions
- Database maintenance.
- Execute database change requests.
- Maintenance of randomization schemes for blinded presentation of data to reviewers.
- Prepare database queries for ad- hoc reports
- Creation of delivery programs
- Creation, testing, verification and implementation of edit check programs
- Code review of colleagues work to ensure consistency and viability of logic
- Provide technical assistance for documentation efforts
- Travel (approximately 5%) domestic and/or international
- 1 – 2 years SQL programming experience
- SAS experience preferred
- Proficiency in Microsoft SQL Server
- Trained in computerized systems in Clinical Trials
- Proficiency in Business computer skills
- Documentation skills
- Thorough knowledge of ICH Guidelines and GCP including regional regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing
- Excellent oral and written communication and presentation skills.
- In depth knowledge of clinical trial process and data management, clinical operations, and systems applications to support operations.
- Demonstrated organizational skills to handle multiple competing priorities simultaneously across an assortment of projects and initiatives.
Application process
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