The Role:
You will be responsible for :
Providing support for executing clinical trials.
Coordinating with the business and as well as onsite staff, clinical research coordinators, principal investigators, and vendors to ensure clinical studies meet or exceed timelines and maintain high quality standards.
Reviewing and monitoring overall clinical data quality and identifying and resolving potential study or site issues.
Implementing study-specific clinical monitoring tools and documents.
Ensuring that all trial protocols are followed accurately.

Ideal Profile:

You have at least 2 years experience including solid experience in a similar role within Not for Profit.
You are highly goal driven and work well in fast paced environments
You are a strong networker & relationship builder
You are a strong team player who can manage multiple stakeholders

Full time, Flexible hours,