Salary: Competitive compensation package for skilled professionals.
Job Description:
We are seeking a dedicated and experienced professional to ensure the timely and high-quality delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).
* 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.
Key Responsibilities:
1. 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.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
4. Continuous Skill Development: Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes.
Requirements:
* 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 skills; ability to multitask and thrive under demanding timelines.