- Do you have at least 2 years of monitoring experience at a CRO or pharma/biotech company?
- KPS Life is hiring CRAs based remotely anywhere in Panama!
The primary responsibility of the Clinical Research Associate (CRA) is to provide monitoring expertise to each Sponsor study they are assigned. The CRA will perform all the tasks related to monitoring and ensuring clinical studies are being performed in accordance with the Sponsor protocol and GCP ICH guidelines.
The CRA will act as the site’s main source of information and performance manager. The CRA will provide support, training, and study procedure knowledge to the sites and study teams to ensure successful conduct and completion of the sponsor’s study.
Candidates must be willing to travel up to 80%
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