Medical Writer

Job not on LinkedIn

🕒 September 4

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥📝 Medical Writer

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 34%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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McKesson

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1833

💼 Consulting

📦 Logistics

🏥 Healthcare

Consulting • Logistics • Healthcare

McKesson is a diversified healthcare leader specializing in pharmaceutical distribution, medical supplies, and healthcare services. Their solutions facilitate patients' access to life-changing therapies, support efficient operations for pharmacies, health systems, and clinics, and address critical issues such as drug shortages through a resilient supply chain. McKesson provides comprehensive services such as pharmacy management software, consulting, and technology solutions for specialty practices, focusing on improving health outcomes and advancing the pharmaceutical industry. They work closely with biopharma companies to enhance medication access, adherence, and commercialization while supporting oncology and biopharma practices through data-driven insights and real-world evidence.

📋 Description

• Research, write, and edit documents across multiple therapeutic areas • Write clinical documents for regulatory submissions, including Clinical Study Protocols, Informed Consents, and Clinical Study Reports • Serve as Medical Writing representative on assigned project teams • Provide timelines for Medical Writing deliverables and input into other departmental deliverables • Manage version control for Medical Writing study deliverables • Identify project challenges, plan or timeline changes, and out-of-scope requests • Suggest solutions to the Project Manager and Sponsor • Perform literature searches and reviews • Serve as primary Sponsor point of contact for clinical document writing • Ensure medical editing review, including copyediting and content review, before external distribution • Perform other duties as assigned

🎯 Requirements

• Bachelor's Degree required • Master's Degree preferred • 3+ years' work experience as a Medical Writer, preferably within the clinical research industry • Experience with oncology clinical trials • Thorough understanding of GCP and ICH guidelines • Advanced user experience with all Microsoft Office products • Adherence to SCRI SOPs and applicable guidance documents • Must be based in the United States • Relocation assistance and visa sponsorship are not available

🏖️ Benefits

• Comprehensive benefits supporting physical, mental, and financial well-being • Competitive compensation package • Annual bonus or long-term incentive opportunities may be offered • Remote work arrangement