Trial Master Files Representative

Triwill Group; Canada; Hybrid; CAD 45,000 - 65,000; Full time

Job summary

Triwill Group, acting on behalf of a partner company, is seeking a Trial Master Files Representative based in Canada. The position is fully remote and focuses on accurate preparation, organization, and maintenance of TMFs for clinical studies.

You will ensure essential study documentation is complete, properly structured, indexed, and maintained according to sponsor expectations, contributing to regulatory readiness and study compliance while collaborating with sponsors, project managers,

Job description

Description:

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Trial Master Files Representative based in Canada.

This remote role supports the accurate preparation, organization, and maintenance of Trial Master Files (TMFs) for clinical research studies.
You’ll help ensure essential study documentation is complete, properly structured, indexed, and maintained according to sponsor expectations.
The position offers the opportunity to work across clinical research teams, sponsors, project managers, monitors, study sites, and other stakeholders.
Your attention to detail will directly contribute to regulatory readiness, study compliance, and high-quality document management.
You’ll operate in a collaborative environment where organization, communication, and reliability are essential to successful study delivery.
The role is well suited to someone who enjoys structured work while managing multiple priorities in a fast-paced clinical research setting.
It also provides an opportunity to deepen your expertise in clinical documentation and Trial Master File processes while working fully remotely.