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Associate Director, Global Regulatory Affairs Operations, Authoring Support
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$200
- At Genmab, we’re committed to building extra(not)ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
- The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
- Coordinates formatting efforts for biologics and drug submissions according to FDA and other global health authorities.
- Technical system skills (e.g. Microsoft Word, ISI Toolbox, Veeva RIM)
- Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.
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