Job Title
Clinical Research Associate - Global Study Monitor
-----------------------------------
About the Role
We are seeking a skilled Clinical Research Associate to join our team in monitoring activities for a global study. The ideal candidate will have experience in site management and be familiar with ICH GCP and applicable clinical trial regulations.
-----------------------------------
Main Responsibilities
The successful candidate will be responsible for:
* Gaining a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
* Managing sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
* Assisting in identifying new potential sites within various therapeutic areas to expand our clinical network.
* Regularly enhancing technical and soft skills to elevate performance and project outcomes.
-----------------------------------
Key Requirements
To be successful in this role, you will need:
* A Bachelor's or Master's degree in a scientific discipline.
* 1-4 years of experience in site monitoring within clinical research.
* Strong understanding of ICH GCP and applicable clinical trial regulations.
* Excellent verbal and written communication skills.
* The ability to multitask and thrive under demanding timelines.
-----------------------------------
What We Offer
This is an excellent opportunity for someone looking to progress their career in clinical research. You will have the chance to work on a global study and develop your skills in site management and monitoring.
As a member of our team, you can expect a challenging but rewarding role with opportunities for professional growth and development.
-----------------------------------