Genmab
Associate Director, Medical Communications and Publications, Solid Tumors
Genmab, Plainsboro, New Jersey, United States
Overview
Associate Director, Medical Communications and Publications, Solid Tumors. The Associate Director of Medical Communications will be responsible for driving the medical communications and publications strategy and activities for assigned Solid tumor asset(s). The individual will play an integral role in leading strategy development, planning, and execution of high-quality scientific publications. This role will collaborate with other functions and departments, including Clinical Development, Clinical Operations, Market Access, Biostatistics, Commercial, Corporate Communications, Translational & Quantitative Sciences and external collaborators to implement the medical communications strategy. Functioning as a member of the Global Medical Affairs department, this individual will report to the Senior Director of Medical Communications and Publications. We have a hybrid model, and onsite presence is required 60% (3 days/week) of the time in Plainsboro, NJ. Responsibilities
Lead the development, implementation, and execution of a global medical communication plan including abstracts, posters, oral presentations, and manuscripts Develop and execute a strategic publication plan: drive strategic publication planning meetings; collaborate with key global cross-functional stakeholders; anticipate risks and identify solutions for publication planning; recognize changes in the healthcare and treatment landscape and adjust publication/communication plans in a timely and efficient manner Serve as the subject matter expert on publication-related matters, working closely with internal and external disease-area experts to ensure high quality analysis, interpretation, communication, and planning of data disclosures Develop scientific content deliverables (including but not limited to scientific communication platform, FAQs) and congress content obtaining insights from key stakeholders, ensuring development of materials aligned with asset and therapeutic area strategy Bring a global perspective and mindset with the ability to work effectively with colleagues and key stakeholders across cultures, backgrounds, and geographies Implement digital enhancements of publications Manage annual budget and resources, ensuring contracts, SOWs and invoices are submitted accurately and timely to ensure high quality deliverables Liaise with agency/vendor partners to ensure timely delivery of quality publication by providing direction, reviewing content, and ensuring processes are consistent with Genmab SOPs Promote and reinforce good publication practices and principles among authors and internal stakeholders ensuring all medical publications are authored, written and reviewed according to GPP and Genmab SOPs Contribute to SOP updates and improvements to achieve organizational goals Qualifications
Advanced degree: PharmD, PhD or MD required. Certification as a Medical Publication Professional (CMPP) desirable Oncology experience strongly preferred 5+ years in medical writing and relevant industry experience or expert in medical communications Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization Understanding of clinical research principles and disease state knowledge Ability to drive and execute within a large matrix, cross-functional team Strategic enterprise thinking with ability to make decisions under ambiguity and tight timelines Understanding of good publication practices and guidance (GPP, ICMJE) and other data communication guidance Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting Strong interpersonal and communication skills Ability to travel domestically and internationally approximately 20% of the time Location and Benefits
Location: Plainsboro, NJ (hybrid model; onsite 60% time). Salary range US-based candidates: see the job posting details; Genmab benefits are provided for regular full-time US employees. About Genmab
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. 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.
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Associate Director, Medical Communications and Publications, Solid Tumors. The Associate Director of Medical Communications will be responsible for driving the medical communications and publications strategy and activities for assigned Solid tumor asset(s). The individual will play an integral role in leading strategy development, planning, and execution of high-quality scientific publications. This role will collaborate with other functions and departments, including Clinical Development, Clinical Operations, Market Access, Biostatistics, Commercial, Corporate Communications, Translational & Quantitative Sciences and external collaborators to implement the medical communications strategy. Functioning as a member of the Global Medical Affairs department, this individual will report to the Senior Director of Medical Communications and Publications. We have a hybrid model, and onsite presence is required 60% (3 days/week) of the time in Plainsboro, NJ. Responsibilities
Lead the development, implementation, and execution of a global medical communication plan including abstracts, posters, oral presentations, and manuscripts Develop and execute a strategic publication plan: drive strategic publication planning meetings; collaborate with key global cross-functional stakeholders; anticipate risks and identify solutions for publication planning; recognize changes in the healthcare and treatment landscape and adjust publication/communication plans in a timely and efficient manner Serve as the subject matter expert on publication-related matters, working closely with internal and external disease-area experts to ensure high quality analysis, interpretation, communication, and planning of data disclosures Develop scientific content deliverables (including but not limited to scientific communication platform, FAQs) and congress content obtaining insights from key stakeholders, ensuring development of materials aligned with asset and therapeutic area strategy Bring a global perspective and mindset with the ability to work effectively with colleagues and key stakeholders across cultures, backgrounds, and geographies Implement digital enhancements of publications Manage annual budget and resources, ensuring contracts, SOWs and invoices are submitted accurately and timely to ensure high quality deliverables Liaise with agency/vendor partners to ensure timely delivery of quality publication by providing direction, reviewing content, and ensuring processes are consistent with Genmab SOPs Promote and reinforce good publication practices and principles among authors and internal stakeholders ensuring all medical publications are authored, written and reviewed according to GPP and Genmab SOPs Contribute to SOP updates and improvements to achieve organizational goals Qualifications
Advanced degree: PharmD, PhD or MD required. Certification as a Medical Publication Professional (CMPP) desirable Oncology experience strongly preferred 5+ years in medical writing and relevant industry experience or expert in medical communications Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization Understanding of clinical research principles and disease state knowledge Ability to drive and execute within a large matrix, cross-functional team Strategic enterprise thinking with ability to make decisions under ambiguity and tight timelines Understanding of good publication practices and guidance (GPP, ICMJE) and other data communication guidance Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting Strong interpersonal and communication skills Ability to travel domestically and internationally approximately 20% of the time Location and Benefits
Location: Plainsboro, NJ (hybrid model; onsite 60% time). Salary range US-based candidates: see the job posting details; Genmab benefits are provided for regular full-time US employees. About Genmab
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. 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.
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