Medical Writer - Remote US

CoverMyMeds; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Medical Writer for a remote US role. You will research, write, and edit clinical documents across therapeutic areas and coordinate with sponsors and internal teams to ensure timely delivery of contracted material.

The position emphasizes writing regulatory submissions (protocols, informed consents, clinical study reports), document version control, and responding to timelines. Remote option with US focus.

Responsibilities

• Write clinical documents for regulatory submissions (protocols, informed consents, study reports).
• Serve as Medical Writing representative on project teams, managing timelines.
• Responsible for document version control of study deliverables.
• Identify project challenges and communicate risks to stakeholders.

Job description

It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

Our Medical Writer will have the overall responsibility for researching, writing, and editing a variety of documents across multiple therapeutic areas. The Medical Writer will work in conjunction with other Sarah Cannon Research Institute departments and Sponsors, as appropriate, for the effective preparation and timely delivery of contracted material.

This is a remote position based in the US; relocation assistance and visa sponsorship are not available.

Job duties include and are not limited to:

• Write clinical documents associated with submissions to regulatory authorities, including but not limited to Clinical Study Protocols, Informed Consents, and Clinical Study Reports
• Serve as the Medical Writing representative on assigned project teams, providing timelines for Medical Writing deliverables and Medical Writing input into other departmental deliverables
• Responsibility for Medical Writing document version control for study deliverables created by the Medical Writing department
• Identify any potential project challenges, including c