Regulatory Documentation Assistant

Regulatory documentation assistant

Digital health MLR refers to the Medical, Legal, and Regulatory review process used to evaluate and approve content before it is released to the users. It is used to ensure that all user-facing materials are accurate, compliant, safe, and aligned with regulatory expectations.

We are seeking a highly motivated, detail-oriented Regulatory documentation assistant to support our team. In this role, you will assist with the preparation, review, and quality assurance (QA) of materials submitted for MLR. Success in this role requires strong English skills, the ability to learn quickly, being agile, fast and oriented to details.

This is an hourly role based on workload – ideal for candidates seeking flexible scheduling, including students who want to gain experience in a digital health technology company.

Responsibilities:

• MLR materials preparation, including decks of program screenshots and annotations
• Review & QA of the materials to ensure meeting the highest quality standards and comply with established guidelines

Requirements:

• Native level or fluent English (mainly written) – must.
• Exceptional attention to details.
• Ability to work both independently and collaboratively.
• Strong organizational skills and comfort using digital tools/platforms.
• Quick learner, agile and fast.
• Excellent communication and interpersonal skills.