Remote Clinical Trial Manager — Operations & Compliance

dicentra Inc.; Canada; Remote; CAD 90,000 - 120,000; Full time

Job summary

dicentra Inc. is seeking an experienced Clinical Trial Manager to oversee active programs, site operations, and monitoring activities. The role can be full-time, part-time fixed-term, or independent consulting, depending on experience.

You will own operational delivery for studies across phases, ensure ICH-GCP compliance, and coordinate with data management and vendors to meet milestones while communicating effectively with sponsors and investigators.

Qualifications

• 5+ years of clinical research experience, with 3+ years in management or senior CRA roles.
• Deep knowledge of ICH-GCP guidelines and health authority requirements.
• Proven ability to drive trials to milestones and manage sponsor relationships.

Responsibilities

• Oversee Phase I–IV studies, site management, and monitoring activities.
• Coordinate data management, vendor interactions, and regulatory submissions.
• Serve as primary contact for sponsors, investigators and external partners.

Skills

Clinical trial mgmt

ICH-GCP knowledge

Project management

Cross-functional collaboration

Sponsor management

Education

Bachelor’s or Master’s degree in Life Sciences

Tools

EDC (Electronic Data Capture)

Job description

dicentra Inc. is seeking an experienced Clinical Trial Manager to oversee active programs, site operations, and monitoring activities. The role can be full-time, part-time fixed-term, or independent consulting, depending on experience.

You will own operational delivery for studies across phases, ensure ICH-GCP compliance, and coordinate with data management and vendors to meet milestones while communicating effectively with sponsors and investigators.