Global Clinical Trial Manager

Moderna; Cambridge (MA); On-site; USD 109,000 - 175,000; Full time

Benefits offered by this job

Competitive healthcare

Well-being resources

Family planning benefits

Generous paid time off

Savings and investments

Location-specific perks

Job summary

Moderna in Cambridge, MA is seeking a Clinical Trial Manager to provide oversight of assigned trials, ensuring quality, compliance and timely delivery. The role involves vendor management, collaboration with Clinical Operations leads, and cross-functional teamwork.

You will draft site materials, monitor data, review monitoring reports, and maintain trial metrics while ensuring adherence to FDA/ICH GCP standards across regions. The position supports UAT testing and may assist across trials.

Qualifications

• 5+ years of trial coordination experience in clinical research.
• Knowledge of FDA and ICH GCP guidelines.
• Experience with cross-functional collaboration and vendors.
• Experience with global clinical operations.
• Strong written and verbal communication.

Responsibilities

• Manage day-to-day oversight of assigned clinical trial(s) across phases.
• Communicate deliverables and timelines to internal teams.
• Manage trial feasibility processes.
• Collaborate with Clinical Operations Leads to execute studies.
• Draft training materials, manuals, and support documentation.
• Monitor clinical data and prepare for data review meetings.
• Review monitoring reports and identify issues.
• Coordinate sample logistics with vendors to meet deliverables.
• Maintain trial metrics and regulatory compliance.
• Support testing of clinical trial systems (e.g., UAT).
• Develop strong relationships with Moderna stakeholders.

Skills

Trial coordination

Global trials experience

Project management

FDA & ICH GCP knowledge

Communication skills

Organizational skills

Education

Bachelor's degree in science

Advanced degree preferred

Job description

Moderna in Cambridge, MA is seeking a Clinical Trial Manager to provide oversight of assigned trials, ensuring quality, compliance and timely delivery. The role involves vendor management, collaboration with Clinical Operations leads, and cross-functional teamwork.

You will draft site materials, monitor data, review monitoring reports, and maintain trial metrics while ensuring adherence to FDA/ICH GCP standards across regions. The position supports UAT testing and may assist across trials.