Social Network for Global Study
Clinical Research Associate positions are available to support a global study in the life sciences industry.
The ideal candidate will have experience in site monitoring and contract research organization (CRO) environments, with a strong understanding of International Conference on Harmonisation Good Clinical Practice (ICH GCP) and clinical trial regulations.
Key responsibilities include delivering high-quality site monitoring activities, managing sites according to regulatory guidelines, identifying new potential sites across various therapeutic areas, and continuously developing technical and soft skills.
The successful candidate will report to the Manager of Clinical Operations and collaborate with site personnel, HR, and administrative staff. They will also be responsible for timely and high-quality reporting and submission of reports to stakeholders.
Education and Experience Requirements
* Bachelor's or Master's degree in a scientific discipline
* 1-4 years of experience in site monitoring within clinical research
Required Skills and Qualifications
The ideal candidate will possess excellent communication skills, be able to multitask under demanding timelines, and have a strong understanding of ICH GCP and clinical trial regulations.
Benefits and Opportunities
This role offers the opportunity to work in a dynamic and rapidly expanding global CRO environment, providing diverse range of clinical development and resource solutions.