Job Description:
The Clinical Research Associate will be responsible for ensuring the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP). This involves gaining a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
Key Responsibilities:
* Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of the SMMP, study protocol, and project plan to ensure 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.