Job Description
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
What's on Offer?
- Excellent career development opportunities
- Flexible working options
- Attractive salary & benefits
Job Tags
Full time, Flexible hours,