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

Similar Jobs