Clinical Data Analyst Jobs

Tempe, AZ

Responsibilities Include:

- Provide input from the data management perspective regarding   the design of clinical trial protocols.
- Design and develop case report forms (CRFs) in accordance with the protocol of a given clinical trial.
- Design and develop CRF instructions in accordance with the protocol and CRF.
- Develop comprehensive data management plans for phase I through phase IV clinical trials.
- Review annotated CRF and participate in database testing.
- Define data validation guidelines, self evident corrections, tracking guidelines, data preparation and data entry guidelines. *Update and maintain, as needed, through the course of the study. *Working in conjunction with the database programmer, develop test data to validate the data check programming.
- Working in conjunction with the database programmer, develop processes for the integration and management of external data such as central labs.
- Provide input from the data management perspective regarding the design case report forms for clinical trials.
- Design the workflow for each project to ensure the timely flow of study data through the processes of data entry, data review, data query and data resolution.
- Program, generate and review status and metric reports as needed.
- Lead and participate in the process of generating queries to study sites when missing, incorrect, or inconsistent data are identified through data review procedures.
- Participate in the coding of adverse events and medications.
- Develop time lines and allocate resources to ensure the completion of project milestones.
- Provide study specific training for the study team

For more information please email: smithhanleyjobs@smithhanley.com