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Associate Director, Medical Communications And Publications, Solid Tumors

5+ years
USD 152,000 – 228,000
10 Dec. 18, 2025
Job Description
Job Type: Full Time 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 and Publications – Solid Tumors | Princeton, NJ

Job ID: R13353
Category: Medical Affairs
Job Type: Full-Time / Hybrid (60% Onsite)
Location: Princeton, New Jersey, United States


About Genmab

Genmab is a global biotechnology leader dedicated to advancing patient outcomes through innovative antibody therapeutics. Over 25 years, the company has developed next-generation platforms including bispecific T-cell engagers, antibody-drug conjugates, immune checkpoint modulators, and effector function-enhanced antibodies.

Headquartered in Copenhagen, Denmark, Genmab operates globally across North America, Europe, and Asia-Pacific. By 2030, the company aims to transform cancer and other serious disease treatment with its Knock-Your-Socks-Off (KYSO®) antibody medicines.

Learn more at www.genmab.com.


Role Overview

The Associate Director of Medical Communications and Publications is responsible for leading and executing the global medical communications and publications strategy for assigned solid tumor assets. This role ensures the development of high-quality scientific content across abstracts, posters, oral presentations, manuscripts, and digital platforms.

Reporting to the Senior Director of Medical Communications and Publications, the Associate Director collaborates with cross-functional teams—including Clinical Development, Clinical Operations, Market Access, Biostatistics, Commercial, Translational & Quantitative Sciences, Corporate Communications, and external partners—to align publication activities with therapeutic and corporate strategies.


Key Responsibilities

  • Lead development and execution of strategic publication plans for assigned solid tumor assets, including congress abstracts, manuscripts, posters, and oral presentations.

  • Drive publication planning meetings, anticipate risks, and implement solutions in a fast-evolving therapeutic landscape.

  • Serve as a subject matter expert (SME) on publication-related matters, collaborating with internal and external stakeholders to ensure scientific accuracy and high-quality deliverables.

  • Develop scientific content for publications, communication platforms, and congress presentations in alignment with therapeutic area strategy.

  • Implement digital enhancements to publications and scientific communications.

  • Manage annual budgets and resources, ensuring timely submission of contracts, statements of work (SOWs), and invoices.

  • Oversee agency/vendor partners to guarantee high-quality publication delivery, adherence to Genmab SOPs, and alignment with Good Publication Practices (GPP).

  • Support SOP development and continuous process improvement within Medical Communications.

  • Bring a global perspective, effectively collaborating across cultures, geographies, and departments.


Required Qualifications

  • Advanced degree: PharmD, PhD, or MD; CMPP certification desirable.

  • Oncology experience strongly preferred.

  • Minimum 5 years of experience in medical writing, publications, or medical communications within the pharmaceutical or biotechnology industry.

  • Expertise in strategic planning and execution of scientific publications across all drug development phases.

  • Understanding of clinical research principles, trial design, statistical methods, and disease state knowledge.

  • Ability to work effectively in a large matrixed, cross-functional team and manage competing priorities.

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

  • Effective interpersonal, leadership, and communication skills.

  • Willingness to travel domestically and internationally (~20%).


Compensation and Benefits (US-Based Candidates)

  • Salary Range: USD 152,000 – 228,000 per year (based on experience, location, and qualifications).

  • Eligibility for discretionary bonuses and long-term incentives.

  • Comprehensive medical, dental, and vision coverage.

  • 401(k) plan with company match.

  • Paid vacation, sick leave, holidays, and 12 weeks of discretionary parental leave.

  • Access to wellness, financial, and lifestyle support programs.

  • Commuter benefits, tuition reimbursement, and Lifestyle Spending Account for wellness and personal expenses.


About You

  • Passionate about scientific communication and advancing oncology research.

  • Strategically minded, with strong planning and execution skills.

  • Collaborative, adaptable, and able to thrive in fast-paced, dynamic environments.

  • Committed to mentoring, process improvement, and enabling high-quality deliverables.

  • Innovative, proactive, and aligned with ethical and regulatory standards.