Research Associate (JR226947)
- Collects and records study data. Inputs all information into database.
- Ensures timely collection of protocol related samples including shipment to outside entities as required.
- Obtains informed consent for non-interventional studies.
- Administers questionnaires.
- Participates and supports investigators in the informed consent process for interventional trials.
- Collects, maintains, and organizes study information including compilation, registration, and submission of data, as required by the Sponsor.
- Attends clinic as needed to perform activities.
- Bachelor's Degree Required, Master's degree preferred.
- ACRP (or SOCRA) certification preferred.
- Ability to use MS Office.
- Good organizing and prioritizing skills.
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