Global Clinical Trials Manager

BioSpace; 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

Discretionary bonus

Job summary

Moderna is seeking a Clinical Trial Manager to provide oversight of assigned trials, ensuring quality, compliance and on-time deliverables. You will manage external vendors and CROs and collaborate with the Clinical Operations team to execute studies worldwide.

The role requires at least 5 years of trial coordination experience, a science-based degree, global trial exposure, strong project management, and a solid understanding of FDA/ICH GCP guidelines.

Qualifications

• At least 5 years of trial coordination experience in a clinical research environment.
• Global trial experience and understanding of drug development.
• Strong project management skills and attention to detail.
• Solid FDA and ICH GCP knowledge to ensure conduct of clinical studies.
• Excellent verbal and written communication.

Responsibilities

• Oversee day-to-day management of assigned trials across all phases.
• Coordinate with internal teams and vendors to meet timelines and deliverables.
• Draft and maintain training materials and trial documentation.
• Monitor data quality and readiness for data review meetings.
• Maintain trial metrics and ensure compliance with Moderna and regulatory standards.
• Support testing of trial systems/databases (e.g., UAT).
• Collaborate with Clinical Operations Lead and study teams.
• Liaise with stakeholders across global sites.

Skills

Clinical trial coordination

Global trial experience

Project management

FDA & ICH GCP knowledge

Communication skills

Attention to detail

Education

Advanced degree preferred

Bachelor's in science

Tools

Clinical trial systems / databases

Job description

Moderna is seeking a Clinical Trial Manager to provide oversight of assigned trials, ensuring quality, compliance and on-time deliverables. You will manage external vendors and CROs and collaborate with the Clinical Operations team to execute studies worldwide.

The role requires at least 5 years of trial coordination experience, a science-based degree, global trial exposure, strong project management, and a solid understanding of FDA/ICH GCP guidelines.