Remote Medical Writer – Oncology Trials

Sarah Cannon Research Institute; Nashville (TN); Remote; USD 70,000 - 110,000; Full time

Benefits offered by this job

Total Rewards package

Bonus or long-term incentives (may be 

Competitive compensation

Job summary

Sarah Cannon Research Institute (SCRI) is a global oncology research organization conducting community-based clinical trials. We advance therapies for patients with cancer and collaborate across 20+ states.

The Medical Writer will research, write, and edit clinical documents, work with Sponsors and cross-functional teams on deliverables, and ensure timely submission readiness. This is a remote position based in the United States; relocation assistance and visa sponsorship are not available.

Qualifications

• Bachelor's Degree required
• Master's Degree preferred
• 3+ years' work experience as a Medical Writer
• Experience with oncology clinical trials
• Thorough understanding of GCP and ICH guidelines
• Advanced user experience with Microsoft Office

Responsibilities

• Write clinical documents for regulatory submissions (Protocols, Informed Consent, Clinical Study Reports)
• Serve as Medical Writing representative on project teams with timelines for deliverables
• Manage document version control for study deliverables
• Identify potential project challenges and propose solutions to PM and Sponsor
• Conduct literature searches to support document development
• Act as primary Sponsor point of contact for assigned project
• Ensure Medical Editing review of drafts before distribution (copyediting and content)
• Perform other duties as assigned

Skills

Medical Writing

Oncology clinical trials

GCP/ICH guidelines

MS Office

SCRI SOPs

Education

Bachelor's Degree

Master's Degree

Job description

Sarah Cannon Research Institute (SCRI) is a global oncology research organization conducting community-based clinical trials. We advance therapies for patients with cancer and collaborate across 20+ states.

The Medical Writer will research, write, and edit clinical documents, work with Sponsors and cross-functional teams on deliverables, and ensure timely submission readiness. This is a remote position based in the United States; relocation assistance and visa sponsorship are not available.