Associate Director, Medical Communications and Publications, CORE Publications
Genmab
9 hours ago
Remote friendly (Plainsboro, NJ)
United States
Medical Affairs
Responsibilities:
- Develop and lead comprehensive global/regional publication strategies and initiatives, including abstracts, congress presentations, and manuscripts for assigned assets/therapeutic areas; provide expertise to the matrix team to execute the medical communication plan.
- Collaborate with cross-functional, key global stakeholders to plan publications; anticipate gaps and identify solutions; monitor changes in the healthcare/treatment landscape and adjust plans timely; ensure alignment with broader medical and CORE publication strategies.
- Serve as a therapy area and product expert for internal and external stakeholders.
- Develop scientific content (including PLS, FAQs) with key stakeholders to address requests from healthcare providers and payers.
- Act as subject matter expert for publication-related matters; work with internal/external disease-area experts to support high-quality analysis, interpretation, communication, and publication planning.
- Collaborate effectively with cross-functional colleagues and key stakeholders across cultures, backgrounds, and geographies.
- Manage annual budget and work within allocated resources; ensure contracts, SOWs, and invoices are submitted accurately and timely.
- Liaise with agency/vendor partners to ensure timely delivery of quality publications; provide direction, review content, and ensure consistent processes with Genmab SOPs.
- Provide subject matter expertise for creation or updates to departmental SOPs to improve/modifying processes and procedures.
Qualifications:
- Advanced degree: PharmD, PhD, DrPH, or MPH required. CMPP certification desirable.
- Knowledge of HEOR/RWE publications; strong understanding of economic modeling, RWE, epidemiological and PRO research.
- 5+ years in medical publications with HEOR, value evidence, or related field in pharmaceutical/biotech.
- Experience across all aspects of scientific publication strategy, planning, and execution across drug development and commercialization.
- Ability to drive and execute in a large matrix, cross-functional team in a fast-paced environment.
- Strategic thinking at an enterprise level; able to make decisions under ambiguity, evolving landscapes, and tight timelines.
- In-depth understanding of good publication practices and guidance (GPP, ICMJE) and scientific data communication guidance.
- Ability to travel domestically/internationally ~20%.
Benefits (as listed in job posting):
- 401(k) plan with 100% match on first 6% of contributions
- Health benefits (two medical options, including HDHP with HSA), dental, and vision
- Voluntary plans: critical illness, accident, hospital indemnity
- Paid time off: vacation, sick leave, holidays; 12 weeks discretionary paid parental leave
- Support resources (backup care, family support programs, financial wellness tools, emotional well-being support)
- Additional perks: commuter benefits, tuition reimbursement, Lifestyle Spending Account
Application instructions:
- Not specified in the provided text.
- Develop and lead comprehensive global/regional publication strategies and initiatives, including abstracts, congress presentations, and manuscripts for assigned assets/therapeutic areas; provide expertise to the matrix team to execute the medical communication plan.
- Collaborate with cross-functional, key global stakeholders to plan publications; anticipate gaps and identify solutions; monitor changes in the healthcare/treatment landscape and adjust plans timely; ensure alignment with broader medical and CORE publication strategies.
- Serve as a therapy area and product expert for internal and external stakeholders.
- Develop scientific content (including PLS, FAQs) with key stakeholders to address requests from healthcare providers and payers.
- Act as subject matter expert for publication-related matters; work with internal/external disease-area experts to support high-quality analysis, interpretation, communication, and publication planning.
- Collaborate effectively with cross-functional colleagues and key stakeholders across cultures, backgrounds, and geographies.
- Manage annual budget and work within allocated resources; ensure contracts, SOWs, and invoices are submitted accurately and timely.
- Liaise with agency/vendor partners to ensure timely delivery of quality publications; provide direction, review content, and ensure consistent processes with Genmab SOPs.
- Provide subject matter expertise for creation or updates to departmental SOPs to improve/modifying processes and procedures.
Qualifications:
- Advanced degree: PharmD, PhD, DrPH, or MPH required. CMPP certification desirable.
- Knowledge of HEOR/RWE publications; strong understanding of economic modeling, RWE, epidemiological and PRO research.
- 5+ years in medical publications with HEOR, value evidence, or related field in pharmaceutical/biotech.
- Experience across all aspects of scientific publication strategy, planning, and execution across drug development and commercialization.
- Ability to drive and execute in a large matrix, cross-functional team in a fast-paced environment.
- Strategic thinking at an enterprise level; able to make decisions under ambiguity, evolving landscapes, and tight timelines.
- In-depth understanding of good publication practices and guidance (GPP, ICMJE) and scientific data communication guidance.
- Ability to travel domestically/internationally ~20%.
Benefits (as listed in job posting):
- 401(k) plan with 100% match on first 6% of contributions
- Health benefits (two medical options, including HDHP with HSA), dental, and vision
- Voluntary plans: critical illness, accident, hospital indemnity
- Paid time off: vacation, sick leave, holidays; 12 weeks discretionary paid parental leave
- Support resources (backup care, family support programs, financial wellness tools, emotional well-being support)
- Additional perks: commuter benefits, tuition reimbursement, Lifestyle Spending Account
Application instructions:
- Not specified in the provided text.