Key Responsibilities of a Clinical Research Associate
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The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and reported data are accurate, complete, and verifiable from source documents.
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Responsibilities include:
* Building relationships with Principal Investigators, study coordinators, pharmacists, and site personnel to ensure efficient management of clinical trials.
* Fostering internal and external customer relationships to ensure timely project delivery as per study requirements and timelines.
* Collaborating with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA) to prepare site essential documents and support ethics and regulatory submission processes.
* Ensuring recruitment of participants as per site target and driving site recruitment and engagement initiatives.
* Monitoring investigational sites as per ICH GCP guidelines including all monitoring visit types across all phases of a clinical trial.
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