Join Genmab as a Senior Medical Writing Manager, where you will lead the creation of impactful clinical documents that support oncology drug development. Collaborate with a dynamic team to drive innovation and quality in a fast-paced environment, making a significant difference in cancer treatment.
Key Responsibilities
Lead the drafting and editing of critical documents
Contribute to Health Authority briefing documents and responses
Drive collaboration with cross-functional trial teams
Provide peer review and editing support
Shape internal processes, tools, and templates
Leverage innovative tools to streamline workflows
Required Qualifications
BA/BS degree in life sciences
At least 7 years of medical or scientific writing experience in the pharmaceutical industry
Experience authoring protocols, investigator’s brochures, and clinical study reports
Solid understanding of clinical development and regulatory frameworks
Preferred Qualifications
Oncology and immunology experience
Experience with AI tools
Knowledge of Health Authority briefing packages and responses
Benefits & Perks
401(k) Plan with 100% match on first 6% of contributionsHealth benefits including medical, dental, and vision insurancePaid vacation, sick leave, and holidays12 weeks of discretionary paid parental leaveAccess to child and adult backup careTuition reimbursementCommuter benefitsLifestyle Spending Account for wellness and personal expenses