A company is looking for a Clinical Project Coordinator (Part-Time).
Key Responsibilities :
Support day-to-day management of studies and ensure timely delivery of project / study tasks
Assist in document management and maintain compliance with regulatory requirements
Prepare and file documents for various study-related meetings and visits
Required Qualifications :
Bachelor's degree in a biomedical-related field, life sciences, or equivalent
Profound knowledge of Good Clinical Practice and relevant regulatory requirements
Commitment to continuous training and knowledge sharing in clinical research
Ability to work independently and as part of a team
Computer literate with a dedication to quality and reliability
Clinical Coordinator • Kansas City, Missouri, United States