Imaging Endpoints, a leading Imaging Technology and Imaging Clinical Research Organisation (iCRO), is seeking a skilled Clinical Project Coordinator to join their team. This role involves coordinating clinical project activities, managing trial master files, and ensuring compliance with regulatory requirements.
🔍About the Role
As a Clinical Project Coordinator, you will play a critical role in supporting the clinical trial team and ensuring the smooth execution of clinical trials.
Your primary responsibilities will include:
Clinical Trial Coordination: Coordinating clinical project activities, including site evaluations, training, and study start-up.
Trial Master File Management: Maintaining trial master files and ensuring project documents are complete, current, and stored appropriately.
Audit Preparation: Preparing for audits and ensuring compliance with regulatory requirements.
Communication: Communicating with sites, project managers, and clients to ensure timely updates and issue resolution.
🎓Requirements
Education: Bachelor’s degree required.
Experience: Experience in the medical or clinical trials industry is preferred.
Skills:
Strong organisational and time management skills.
Proficiency in MS Office and internet applications.
Knowledge of Good Clinical Practice (GCP) and Quality Assurance/Compliance in a clinical trials setting is preferred.
💎What We Offer
Career Growth: Opportunities for professional development and growth in a leading iCRO.
Collaborative Environment: A dynamic and supportive team environment.
Competitive Benefits: Competitive salary and benefits package.
🌟Why Choose Imaging Endpoints?
Mission-Driven: Opportunity to work with a company passionate about connecting imaging to the cure.
Global Team: Collaborative and dynamic team environment with growth opportunities.
Innovative Culture: A company that values innovation, quality, and people.
👉 Apply Here: 🔗 Click to Apply on LinkedIn