Skillful and diligent professionals are sought after to assume key responsibilities in ensuring the timely and high-quality delivery of site monitoring activities.
The ideal candidate will possess a strong understanding of clinical research principles, regulatory requirements, and project management best practices.
* Deliver Site Monitoring Plans: Ensure adherence to quality and timelines by gaining a comprehensive understanding of the site monitoring master plan, study protocol, and project plan.
* Site Management Compliance: Manage sites according to relevant regulations to minimize Quality Assurance (QA) audit observations.
* Continuous Skill Development: Regularly enhance technical and soft skills to improve performance and project outcomes.
Candidates with 1-4 years of experience in site monitoring within clinical research are preferred. A Bachelor's or Master's degree in a scientific discipline is also required.
Excellent verbal and written communication skills, multitasking abilities, and the capacity to thrive under demanding timelines are essential for success in this role.
Primary Responsibilities:
We are looking for skilled professionals to take on the following responsibilities:
1. Deliver Site Monitoring Plans: Gain a comprehensive understanding of the site monitoring master plan, study protocol, and project plan.
2. Site Management Compliance: Manage sites according to relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites within various therapeutic areas.
4. Continuous Skill Development: Regularly enhance technical and soft skills to improve performance and project outcomes.