Elevate your medical writing career with an Oncology Medical Writer II role in the pharmaceutical industry. Contribute to clinical documents and collaborate with cross-functional teams as you develop your skills.
This position requires a university or advanced degree in a scientific discipline and involves participating in document planning, writing complex documents like Phase 1/2 CSRs, and participating in meetings. You'll gain experience in regulatory standards while working under supervision and guiding junior writers. Embrace your growth in this team-oriented environment.
Key Responsibilities:
• Write basic clinical documents, including protocols and narratives
• Contribute to low to medium complexity regulatory documents
• Perform document QC and conduct literature searches
• Participate in planning and review meetings
• Mentor junior staff on writing processes and best practices
Requirements:
• Minimum 2 years of pharmaceutical/scientific experience