Job Title: Clinical Research Associate
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Description:
The primary purpose of this role is to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP). This involves a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
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Key Responsibilities:
* Deliver on the Site Monitoring Plan: Gain a thorough understanding of the SMMP, study protocol, and project plan to guarantee adherence to quality and timelines.
* Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
* Site Identification: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
* Continuous Skill Development: Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes.