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Parexel FSP is seeking a Clinical Trial Coordinator to support trial administration, document management, and regulatory tasks from anywhere in the United States. You will work with site staff and internal teams to ensure timely data collection, filing, and study tracking in CTMS.
The role requires 1–2 years in clinical research, proficiency with MS Office, strong communication, and the ability to work independently in a matrix, multicultural environment, while following GCP and Parexel SOPs.
Parexel FSP is seeking a Clinical Trial Coordinator to support trial administration, document management, and regulatory tasks from anywhere in the United States. You will work with site staff and internal teams to ensure timely data collection, filing, and study tracking in CTMS.
The role requires 1–2 years in clinical research, proficiency with MS Office, strong communication, and the ability to work independently in a matrix, multicultural environment, while following GCP and Parexel SOPs.