Clinical Trial Manager

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee external vendors and contract research organizations.

• Support the development of protocols and the completion of study reports.

• Organize and take part in investigator meetings.

• Maintain the trial master file.

⛳️ Requirements

• Manage individual clinical trials and/or programs effectively.

• Create study documents, including the Monitoring Manual and Study Operations Manual.

• Coordinate the creation of study materials such as CRFs and patient diaries.

• Ensure compliance with Good Clinical Practices (GCPs), standard operating procedures (SOPs), and study protocols.

• Provide direction to Clinical Research Associates (CRAs).

• Monitor patient enrollment and execute closeout activities.

• Negotiate contracts with vendors providing clinical trial services.

• Ensure regulatory compliance at investigational sites.

🏝️ Benefits

• Health insurance coverage.

• Flexible work arrangements available.

• Opportunities for professional development.