🏡 Remote (U.S. Based)
💼 Full-Time | Contract-to-Hire Potential
💰 Annual Range: $84,400 – $211,100
📍 Location: Remote U.S. (IQVIA HQ in Durham, NC)
📝 Overview:
IQVIA is seeking a Senior Medical Writer to lead the creation of high-quality regulatory and clinical documentation. This role blends leadership, communication, and scientific expertise to support global drug development. If you thrive under deadlines, mentor with intention, and have a sharp eye for regulatory precision, this is your lane.
🧩 Key Responsibilities:
• Lead the development of protocols, clinical study reports (CSRs), and more
• Coordinate timelines, templates, and customer interactions
• Deliver constructive feedback and mentor junior writers
• Present medical writing process in internal or bid defense meetings
• Manage budgets, project timelines, and client communication
• Interpret and summarize complex data clearly and concisely
📚 What You’ll Need:
• 🎓 Bachelor’s (required), Master’s (preferred), or Ph.D. (ideal) in life sciences
• ✍️ 5+ years of relevant medical writing experience
• 🧠 Deep understanding of GCP, drug development, and regulatory docs
• 📈 Strong grasp of clinical statistics and data interpretation
• 🗣 Excellent written and verbal communication skills
• 🧮 Budgeting, forecasting, and project planning experience
• 🧘 Confidence, initiative, and the ability to deliver under pressure
🌍 Bonus Points For:
• Proven leadership in cross-functional writing projects
• Biopharma client-facing experience
• Experience mentoring or developing training for others
• Bilingual fluency is a plus
💡 Why IQVIA?
At IQVIA, we don’t just write—
We translate science into purpose.
As a global leader in healthcare intelligence, we support the development of life-saving therapies with innovation, impact, and integrity. Your words can change lives here.
📲 Apply now and join a team where your knowledge becomes a bridge between science and healing.