
Associate Director, Medical Writer – Publications
Posted Aug 6

Posted Aug 6
This is a fully remote position, open to applicants in United States.
• Direct the tactical implementation of publications derived from global medical affairs publication strategies.
• Influence the external scientific dialogue.
• Ensure that data is conveyed with precision, clarity, and impact through high-quality publications and conference materials.
• Create strategic, high-impact scientific publications and conference materials focused on oncology.
• Work collaboratively with cross-functional teams and external experts.
• Comply with GPP, ICMJE guidelines, global compliance standards, BeOne SOPs, work instructions, and quality benchmarks.
• Manage and prioritize multiple concurrent projects across different regions.
• Build and sustain relationships with internal colleagues, external authors, journal editors, publishers, and other professional organizations.
• Supervise publication agencies and actively engage in publication steering committees.
• An advanced degree (PhD, PharmD, MD, or MS) in life sciences or a related discipline.
• Specialization in oncology is highly preferred.
• A minimum of 5–7 years of pertinent medical writing experience.
• Strong focus on global publication planning and conference communications.
• Experience within the biotechnology/pharmaceutical industry or at a medical communications agency is essential.
• Exceptional written and verbal communication abilities.
• A sharp attention to scientific accuracy and editorial quality.
• Experience in working globally, cross-functionally, and across cultures.
• Proven track record in developing strategic, high-impact scientific publications and conference materials in oncology.
• Extensive experience collaborating with cross-functional teams and external experts in a biotech or pharmaceutical environment.
• In-depth knowledge of and compliance with GPP, ICMJE guidelines, and global compliance standards in medical publications.
• Strong project management capabilities.
• Familiarity with global regulatory and medical affairs contexts (e.g., US, EU, APAC).
• Prior experience in writing publications related to clinical oncology and/or health economics and outcomes research in oncology is preferred.
• Experience in overseeing publication agencies and participation in publication steering committees is preferred.
• Active membership in ISMPP, AMWA, EMWA, or similar organizations is preferred.
• Eligibility for an annual bonus plan for Non-Commercial roles.
• Discretionary equity awards.
• Employee Stock Purchase Plan.
• Medical insurance.
• Dental insurance.
• Vision insurance.
• 401(k) plan.
• FSA/HSA options.
• Life Insurance coverage.
• Paid Time Off.
• Wellness programs.
• Work-related travel approximately 5-10%.
Novo Nordisk
Novo Nordisk
Catalight
IQVIA
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