Associate Director, Medical Writing

Genmab is seeking an Associate Director, Medical Writing to contribute to the medical writing portfolio within the clinical and regulatory areas, authoring briefing documents, clinical trial medical synopses, protocols, and other clinical documentation. The role requires a strategic thinker with excellent communication skills, and the ability to manage multiple tasks simultaneously.

Requirements

• Independently author and review complex clinical and regulatory documents
• Draft and edit more strategic documents, such as Health Authority briefing books and publications
• Represent medical writing on internal teams
• Lead submission team activities and oversee the preparation of critical documents
• Facilitate team participation in document preparation, including scheduling meetings, developing timelines, and managing document reviews and decisions
• Maintain up-to-date knowledge of relevant regulatory guidelines and requirements
• Adhere to guidelines, SOPs, practices, and technical standards in all aspects of work

Benefits

• 401(k) Plan with 100% match on the first 6% of contributions
• Health Benefits, including two medical plan options, dental, and vision insurance
• Voluntary Plans, including critical illness, accident, and hospital indemnity insurance
• Time Off, including paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
• Support Resources, including access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
• Additional Perks, including commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses