Job Description
The Offer
- Excellent career development opportunities
- Flexible working options
- Attractive salary & benefits
The Job
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.
The 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
The Employer
Conserve. Advocate. Restore. Educate. Keeping our client Since 1931! They need you to support their mission to conserve and restore wildlife and habitat through education and advocacy!
Job Tags
Full time, Flexible hours,