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Clinical Data Programmer I
2 months ago
**Minimum Qualifications & Experience**:
Graduate in information science or life science related field, or similar. Preferably at least six months to three years’ experience in a similar role in a CRO or pharmaceutical company
**Responsibilities**
The CDP-I shall be responsible for programming activities on a project. This shall include designing andimplementation of clinical database, programming of data review listings andprogramming of data reconciliation. The CDP-I shall ensure quality standards per SOPs and ICH-GCP.
Participates in project team meetings as required.
2. Perform database design and creation of entry screens per the design specifications for a project. This will also include alpha testing before releasing.
3. May assist in edit check programming per the edit check specifications fora project. This will also include alpha testing before releasing.
4. Perform data mapping/reconciliation programming per the data mapping/reconciliation specifications for a project. This will also include alpha testing before releasing.
5. Perform data listing programming per the data listing specifications for a project.
This will also include alpha testing before releasing.
6. Performs status report setup and programming per the status report specifications fora project. This will also include alpha testing before releasing.
7. The CDP-I may be requested to provide some programming related technical support on projects.
8. The CDP-I may be requested to provide some trouble shooting and problem solving related to programming on projects.
10. Perform external dataloads, i.e. labs, ECGs etc., as needed.
11. Support the Project/Programming Lead on aproject on tasks as needed.
12. Ensure all programming activities and processes performed are conducted in accordance with standard operating procedures and good programming practices.
13. Support in the validation of electronic systems, software and programs implemented in accordance with current regulatory requirements.
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