Job Description:
We are seeking skilled professionals to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).
Key Responsibilities:
* Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of the Site Monitoring Master Plan (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.
Work Relations:
* Report to the Manager of Clinical Operations: Collaborate with site personnel, HR, site leads, and administrative executives.
Your Key Contributions:
* Timely and high-quality execution of site monitoring activities
* Prompt report generation and submission to stakeholders
Required Skills and Qualifications:
* Education: Bachelor's or Master's degree in a scientific discipline
* Experience: 1-4 years of experience in site monitoring within clinical research
* Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and thrive under demanding timelines