Overview:
The Research Associate I assists the Study Director with the planning, execution, data tabulation, and reporting of non-Good Laboratory Practices (GLP) and GLP Toxicology, Medical Device and Pharmacokinetic studies.
Responsibilities:
- Responsible for the preparation of study notebooks.
- Creates and reviews raw data collection forms for adherence to protocol and clarity/efficacy prior to study start.
- Assists with the creation and review of study event calendars/schedules.
- Confirms study activities are scheduled with the in-life team as described by the protocol.
- Assists the Study Directors in coordinating study conduct and ensuring proper raw data collection according to the…
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