Project Coordinator
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Job Summary
To support clinical study operations, the full-time Project Coordinator will manage study details in CTMS and GoClinical, coordinate site communications and logistics, and assist with document creation and audits while working remotely.
Key responsibilities
- Create and maintain study details in CTMS and GoClinical, including contact information and issue tracking
- Serve as the main point of contact for site communications and activity coordination
- Assist with the development of study documents and training materials as needed
Required qualifications
- Bachelor's degree or equivalent experience with a minimum of 3 years in a related field
- At least 2 years of experience in clinical study, research, or healthcare
- Current knowledge of ICH/GCP regulations and guidelines
- Proficiency in Microsoft Office and Adobe Acrobat applications
- Strong organizational skills with the ability to multitask effectively
Complete Job Description
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