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Associate Director, Medical Communications And Publications, Solid Tumors

Genmab
Genmab
5+ years
USD 152,000 – 228,000
10 Jan. 1, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director – Medical Communications & Publications (Solid Tumors)

Location: Princeton / Plainsboro, New Jersey, USA
Job Category: Medical Affairs – Medical Communications & Publications
Job Type: Full-Time | Hybrid (60% Onsite)
Experience Required: 5+ Years
Job ID: R13353

Company Overview

Genmab is a global biotechnology company dedicated to transforming the lives of patients through innovative and differentiated antibody-based medicines. With a strong scientific foundation and a robust oncology pipeline, Genmab focuses on delivering breakthrough therapies across cancer and other serious diseases. Headquartered in Copenhagen, Denmark, Genmab operates globally across North America, Europe, and Asia-Pacific.

Position Overview

Genmab is seeking an Associate Director, Medical Communications and Publications to lead global publication strategy and execution for assigned Solid Tumor oncology assets. This role sits within Global Medical Affairs and is responsible for driving high-quality scientific communications across the product lifecycle, from clinical development through commercialization.

The role requires strong cross-functional leadership, strategic thinking, and deep expertise in medical publications, oncology, and scientific data dissemination. The Associate Director will report to the Senior Director, Medical Communications & Publications and collaborate closely with internal stakeholders and external partners.

Key Responsibilities

  • Lead the global medical communications and publications strategy including abstracts, posters, oral presentations, and peer-reviewed manuscripts

  • Drive strategic publication planning meetings and proactively identify risks, mitigation strategies, and opportunities

  • Serve as the subject matter expert for publication-related activities, ensuring scientific accuracy, quality, and compliance

  • Develop scientific communication platforms, FAQs, congress materials, and data disclosure content aligned with asset strategy

  • Collaborate cross-functionally with Clinical Development, Biostatistics, Market Access, Commercial, Corporate Communications, and external collaborators

  • Ensure adherence to Good Publication Practice (GPP), ICMJE guidelines, and internal SOPs

  • Oversee publication agencies and vendors, including scope of work, timelines, quality, and budget management

  • Implement digital and innovative enhancements to publication dissemination

  • Contribute to the development and continuous improvement of medical communications SOPs and processes

  • Manage annual publication budgets and ensure accurate, timely financial documentation

Qualifications & Experience

  • Advanced degree required: PharmD, PhD, or MD

  • CMPP certification preferred

  • 5+ years of experience in medical writing, medical communications, or scientific publications within the pharmaceutical or biotech industry

  • Strong oncology experience, preferably in solid tumors

  • Demonstrated expertise in publication strategy across all phases of drug development

  • Solid understanding of clinical trial design, statistical methods, and data interpretation

  • Proven ability to operate effectively in a matrixed, global environment

  • Strong strategic thinking, communication, and stakeholder management skills

  • Knowledge of GPP, ICMJE, and regulatory guidance related to scientific communications

  • Ability to travel domestically and internationally up to 20%

Work Model

Hybrid work model with 60% onsite presence (3 days/week) at the Plainsboro, NJ office.

Compensation (US-Based Candidates)

Salary Range: USD 152,000 – 228,000 per year
Compensation may include discretionary bonuses and long-term incentives based on role eligibility, experience, and location.

Employee Benefits

  • Competitive compensation and incentive programs

  • 401(k) with company match

  • Comprehensive medical, dental, and vision insurance

  • Paid parental leave, vacation, sick leave, and holidays

  • Wellness, mental health, and financial support programs

  • Tuition reimbursement and lifestyle spending accounts

  • Flexible and inclusive work culture focused on long-term career growth

Why Join Genmab

At Genmab, science drives everything we do. You will join a globally respected organization committed to innovation, integrity, and improving patient outcomes through next-generation antibody therapies. This role offers the opportunity to shape global scientific communication strategies that influence oncology practice worldwide.

Apply Now to advance your career in Medical Affairs, Oncology Publications, and Scientific Communications with a global biopharmaceutical leader.