π Core Information
πΉ Job Title: Associate Director, Medical Communications and Publications, Solid Tumors
πΉ Company: Genmab
πΉ Location: Princeton, New Jersey, United States
πΉ Job Type: Full-Time, Hybrid (On-site 60% of the time)
πΉ Category: Biotechnology Research
πΉ Date Posted: May 15, 2025
πΉ Experience Level: 5-10 years
πΉ Remote Status: On-site majority of the time
π Job Overview
Key aspects of this role include:
- Driving medical communications and publications strategy for assigned solid tumor assets
- Collaborating with cross-functional teams to implement medical communications strategy
- Leading the development, implementation, and execution of a global medical communication plan
- Serving as the subject matter expert on publication-related matters
- Bringing a global perspective and mindset to work effectively with colleagues across cultures and geographies
ASSUMPTION: This role requires a high level of strategic thinking, cross-functional collaboration, and global mindset to ensure high-quality scientific publications and effective communication of data disclosures.
π Key Responsibilities
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Lead the development, implementation, and execution of a global medical communication plan including abstracts, posters, oral presentations, and manuscripts
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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
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Develop scientific content deliverables and congress content, obtaining insights from key stakeholders to ensure materials are aligned with overall asset and therapeutic area strategy
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Implement digital enhancements of publications and manage annual budget, ensuring contracts, SOWs, and invoices are submitted accurately and in a timely manner
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Liaise with agency/vendor partners to ensure timely delivery of quality publications, providing direction, reviewing developed content, and ensuring process is consistent with Genmab SOPs
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Promote and reinforce good publication practices and principles among authors and internal stakeholders, ensuring all medical publications are being authored, written, and reviewed according to GPP and Genmab SOPs
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Bring subject matter expertise in discussions regarding the creation or updates to departmental SOPs, improving/modifying processes and procedures to help achieve organizational goals
ASSUMPTION: This role involves a high degree of strategic planning, cross-functional collaboration, and attention to detail to ensure the successful execution of medical communications and publications.
π― Required Qualifications
Education: Advanced degree (PharmD, PhD, or MD) required. Certification as a Medical Publication Professional (CMPP) desirable.
Experience: 5+ years in medical writing and relevant industry work experience and/or expert in medical communications, preferably in oncology
Required Skills:
- Expertise across all aspects of scientific publication strategy, planning, and execution during all phases of drug development and commercialization process
- Demonstrate an understanding of clinical research principles and disease state knowledge
- Ability to drive and execute within a large matrix, cross-functional team
- Proven ability to think strategically at an enterprise level and make decisions even under conditions of ambiguity, evolving landscapes, fast-paced, and tight timelines
- Understanding of good publication practices and guidance (GPP, ICMJE), and other guidance related to scientific data communication
- Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting
- Effective interpersonal and communication skills
- Ability to travel domestically and internationally approximately 20% of the time
Preferred Skills:
ASSUMPTION: Given the role's focus on medical communications and publications, candidates should have a strong background in scientific writing, strategic planning, and cross-functional collaboration within the biotechnology industry.
π° Compensation & Benefits
Salary Range: $152,000.00 - $228,000.00 per year (USD)
Benefits:
- Health Insurance
- Retirement Plan
- Paid Time Off
- Flexible Work Hours
Working Hours: Full-time, with flexible hours and a hybrid work arrangement (on-site 60% of the time)
ASSUMPTION: The salary range provided is based on the company's job posting and is typical for this role and experience level in the biotechnology industry. Benefits are standard for the industry and reflect the company's commitment to employee well-being.
π Applicant Insights
π Company Context
Industry: Biotechnology Research
Company Size: 1,001-5,000 employees
Founded: 1999
Company Description:
- Genmab is an international biotechnology company dedicated to improving the lives of patients through innovative and differentiated antibody therapeutics
- The company has a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators, and effector function-enhanced antibodies
- Genmab is committed to building extra[not]ordinary futures together, with a passionate, innovative, and collaborative team
Company Specialties:
- Antibody therapeutics
- Biotechnology research
- Cancer treatment
- Serious diseases
Company Website: http://www.genmab.com
ASSUMPTION: Genmab is a well-established biotechnology company with a strong focus on innovative antibody therapeutics, making it an attractive employer for professionals in the field.
π Role Analysis
Career Level: Mid-level to senior-level management
Reporting Structure: Reports to the Senior Director of Medical Communications and Publications
Work Arrangement: Hybrid, with on-site presence required 60% of the time (3 days/week) in Plainsboro, NJ
Growth Opportunities:
- Potential advancement to a senior-level role within the Medical Affairs department
- Expansion of responsibilities as the company's pipeline grows and evolves
- Opportunities to work on diverse therapeutic areas and assets
ASSUMPTION: This role offers significant growth potential within the Medical Affairs department and the broader organization, as Genmab continues to expand its pipeline and global presence.
π Location & Work Environment
Office Type: Hybrid, with on-site presence required 60% of the time
Office Location(s): Plainsboro, New Jersey, United States
Geographic Context:
- The Princeton area offers a mix of urban and suburban living, with easy access to New York City and Philadelphia
- The region is home to a thriving biotechnology industry, with numerous companies and research institutions
- Genmab's office is located in the Princeton Corporate Center, providing a convenient and professional work environment
Work Schedule: Full-time, with flexible hours and a hybrid work arrangement
ASSUMPTION: The hybrid work arrangement and convenient office location allow for a good work-life balance, while still providing opportunities for in-person collaboration and networking within the biotechnology industry.
πΌ Interview & Application Insights
Typical Process:
- Phone or video screen with the hiring manager
- On-site or virtual interview with cross-functional stakeholders
- Final interview with the senior director or another senior leader
Key Assessment Areas:
- Strategic thinking and problem-solving skills
- Cross-functional collaboration and communication skills
- Expertise in medical communications and publications
- Alignment with Genmab's mission, values, and company culture
Application Tips:
- Highlight relevant experience and achievements in medical communications and publications
- Tailor your resume and cover letter to emphasize your fit for the role and Genmab's mission
- Prepare for behavioral and situational interview questions focused on strategic planning, cross-functional collaboration, and problem-solving
ATS Keywords: Medical Communications, Publications Strategy, Scientific Writing, Oncology Experience, Cross-Functional Collaboration, Clinical Research, Publication Planning, Data Analysis, Interpersonal Skills, Project Management, Budget Management, Digital Enhancements, Good Publication Practices, SOP Development, Strategic Thinking, Problem Solving
ASSUMPTION: The interview process will focus on assessing the candidate's strategic thinking, cross-functional collaboration, and expertise in medical communications and publications, with a strong emphasis on cultural fit and alignment with Genmab's mission and values.
π οΈ Tools & Technologies
- Microsoft Office Suite (Word, PowerPoint, Excel)
- PubMed
- ClinicalTrials.gov
- Medical writing and publication software (e.g., VantagePoint, Editage)
ASSUMPTION: The required tools and technologies for this role are standard in the biotechnology industry and reflect the need for effective communication, collaboration, and data management in medical communications and publications.
π Cultural Fit Considerations
Company Values:
- Passion for innovation
- Determination
- Integrity
- Working as one team and respecting each other
Work Style:
- Collaborative and cross-functional
- Data-driven and strategic
- Agile and adaptable
- Results-oriented and accountable
Self-Assessment Questions:
- Do you have a proven track record of driving strategic publication planning and execution in a matrix, cross-functional team environment?
- Are you comfortable working with diverse stakeholders across cultures, backgrounds, and geographies?
- Do you thrive in an agile, fast-paced work environment with evolving landscapes and tight timelines?
ASSUMPTION: Genmab values a collaborative, data-driven, and agile work environment, with a strong emphasis on innovation, determination, and integrity. Candidates should assess their fit with these values and work style preferences before applying.
β οΈ Potential Challenges
- Managing multiple stakeholders and balancing competing priorities in a matrix, cross-functional team environment
- Keeping up with the fast-paced and evolving biotechnology industry, as well as changes in the healthcare and treatment landscape
- Adapting to a hybrid work arrangement and maintaining effective communication and collaboration with remote team members
- Travel requirements (approximately 20% of the time)
ASSUMPTION: These challenges reflect the dynamic and fast-paced nature of the biotechnology industry, as well as the need for effective communication, collaboration, and adaptability in a hybrid work environment.
π Similar Roles Comparison
- Compared to other Medical Communications roles, this position offers a unique focus on solid tumor assets and a strong emphasis on strategic publication planning and execution
- In the biotechnology industry, Genmab is known for its innovative antibody therapeutics and commitment to improving the lives of patients, making it an attractive employer for professionals in the field
- Career progression in Medical Affairs typically involves moving into senior-level roles or expanding responsibilities as the company's pipeline grows and evolves
ASSUMPTION: This role offers a unique focus on solid tumor assets and strategic publication planning, with significant growth potential within the Medical Affairs department and the broader organization.
π Sample Projects
- Developing and executing a global medical communication plan for an assigned solid tumor asset, including abstracts, posters, oral presentations, and manuscripts
- Collaborating with cross-functional stakeholders to create scientific content deliverables and congress content aligned with overall asset and therapeutic area strategy
- Implementing digital enhancements of publications and managing annual budget, ensuring contracts, SOWs, and invoices are submitted accurately and in a timely manner
ASSUMPTION: These sample projects reflect the strategic, cross-functional, and data-driven nature of the role, as well as the need for effective communication, collaboration, and project management skills.
β Key Questions to Ask During Interview
- How does this role fit into the overall medical communications and publications strategy for the assigned solid tumor asset(s)?
- What are the key priorities for this role in the first 30, 60, and 90 days?
- How does Genmab support the professional development and growth of its employees in Medical Affairs?
- What is the typical career progression for someone in this role, and what opportunities exist for growth within the department and the broader organization?
- How does Genmab foster a collaborative and inclusive work environment, particularly in a hybrid setting?
ASSUMPTION: These interview questions focus on understanding the role's strategic fit, priorities, and growth opportunities, as well as Genmab's commitment to professional development and collaboration in a hybrid work environment.
π Next Steps for Applicants
To apply for this position:
- Submit your application through this link
- Tailor your resume and cover letter to emphasize your fit for the role and Genmab's mission
- Prepare for behavioral and situational interview questions focused on strategic planning, cross-functional collaboration, and problem-solving
- If selected for an interview, be ready to discuss your relevant experience and achievements in medical communications and publications, as well as your alignment with Genmab's mission, values, and company culture
- Follow up with the hiring manager or HR representative within one week of your interview to express your interest in the role and reiterate your qualifications
β οΈ This job description contains AI-assisted information. Details should be verified directly with the employer before making decisions.