At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.
Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.
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The Role
Are you ready to make a meaningful impact in oncology drug development and be part of a dynamic, collaborative team that values innovation, quality, and scientific integrity? At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart of a team that plays a critical role in bringing innovative therapies to patients-and we want you to grow with us.
As part of our Global Medical Writing team, you will drive the development of high-quality clinical documents to support operational, medical, and regulatory activities across the Genmab portfolio. You will help craft scientifically robust arguments, collaborate across functions, and shape messaging that resonates with diverse stakeholders. You will also be involved in developing processes and tools to support further development of the department.
The ideal candidate is a strategic thinker with strong analytical skills, scientific rigor, and a commitment to excellence. You thrive in a fast-paced environment, are motivated by high standards, and can lead projects with both independence and collaboration. You're proactive, flexible, and highly organized, with the ability to juggle multiple priorities while keeping the bigger picture in focus. If you're detail-oriented, results-driven, and excited about using your skills to make a difference-while exploring cutting-edge tools like AI-you'll fit right in.
Responsibilities
- Lead the drafting and editing of critical documents such as protocols, investigator's brochures, and clinical study reports.
- Contribute to Health Authority briefing documents and responses, and clinical modules of regulatory submissions (e.g., NDA, BLA, MAA).
- Drive collaboration with cross-functional trial teams to manage timelines, facilitate meetings, and lead review cycles.
- Provide expert peer review and editing support to elevate the quality of documents across the team.
- Help shape internal processes, tools, and templates-bringing your insights to enhance how we work.
- Leverage innovative tools, including AI-driven platforms, to streamline writing and analysis workflows.
Requirements
- BA/BS degree in life sciences and at least 7 years of medical or scientific writing experience, in the pharmaceutical industry. Oncology and immunology experience preferred
- Demonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates should also have knowledge of Health Authority briefing packages, Health Authority responses, and Pediatric Investigational Plans (PIPs).
- Experience authoring clinical components of regulatory submission (NDA, BLA, MAA) highly preferred.
- Solid understanding of clinical development and regulatory frameworks, including GCP and ICH guidelines.
- Proficiency with writing tools such as MS Word, EndNote, document management systems
- Ability to interpret and summarize tabular and graphical data presentations.
- Experience with AI tools preferred
About You - additional qualities you bring to the table
- You are capable of working on multiple tasks and shifting priorities, and leading cross-functional teams under strict timelines.
- You are motivated and detail-oriented.
- You have the ability to work across all trial phases and prioritize your own tasks.
- You are a dedicated team player and a great communicator with excellent oral and written communication skills.
- You are proactive and open-minded
- You have a quality mindset and thrive in a fast-paced and changing environment.
- You are result- and goal-oriented and committed to contributing to the overall success of Genmab.
For US based candidates, the proposed salary band for this position is as follows:
$126,240.00 - $189,360.00
The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.
When you join Genmab, you're joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:
- 401(k) Plan: 100% match on the first 6% of contributions
- Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
- Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
- Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
- Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
- Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses
About You
- You are genuinely passionate about our purpose
- You bring precision and excellence to all that you do
- You believe in our rooted-in-science approach to problem-solving
- You are a generous collaborator who can work in teams with a broad spectrum of backgrounds
- You take pride in enabling the best work of others on the team
- You can grapple with the unknown and be innovative
- You have experience working in a fast-growing, dynamic company (or a strong desire to)
- You work hard and are not afraid to have a little fun while you do so!
Locations
Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.
About Genmab
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.
Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.
Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).
Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.