Associate Director Medical Writing Jobs in New Jersey
Associate Director Medical Writing jobs in New Jersey are open across Princeton, Madison, and Nutley and other New Jersey metros, with employers like Celgene Corporation, Juno Therapeutics, and Eisai hiring at every experience level. Find a role that fits below and apply directly.
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Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Position Summary
The primary responsibility of the Associate Director for IO Lung Cancer in Global Medical Oncology, is to develop and implement the Global/US Medical strategies and objectives in Lung Cancer, specifically in non-metastatic lung cancer, as they relate to nivolumab and ipilimumab. This role is responsible for integrating and aligning tumor strategies by establishing and maintaining cross-functional collaborative relationships with key stakeholders, including, but not limited to, US Commercialization, Global Medical, Clinical Development, and Medical Capabilities teams.
Key Responsibilities
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Collaborate with the Medical Product Lead with the development and implementation of the GMO medical plan that drives product differentiation, lifecycle management as well as advancing disease specific strategies in alignment with Commercialization and R&D, translating strategies into meaningful impact for patients.
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Provide strategic, scientific, and executional leadership while partnering with the integrated matrix team, including Medical Communications, Evidence Generation, Commercial, Field Medical, R&D, GPT and Access teams.
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Develop/refine and implement key medical activities, including medical advisory boards, Scientific Engagement Partner resources and training, congresses, reactive content, and communication strategy, including publications.
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Implement data generation strategies and collaborate with Medical Evidence Generation (MEG) to oversee the execution of the Investigator-Sponsored Research (ISR) programs from concept through full execution, including reporting the evidence at scientific congresses, in peer-reviewed publications, and proactive/reactive BMS communication tools.
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Collaborate within Medical matrix teams to plan and deliver overall medical objectives with flawless execution and budget utilization.
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Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines is understood and communicated properly internally and externally, as they relate to areas of scope and responsibility.
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Develop and maintain long-term, trusted relationships with external Thought Leaders and scientific experts to assess unmet medical needs and develop appropriate medical strategies.
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Ensure medical strategies, objectives, and tactics are aligned across the medical matrix and integrated with the strategic brand plan.
Qualifications & Experience
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Advanced scientific degree (PharmD, MD, PhD)
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Prior (5+ years) pharmaceutical industry experience in medical affairs is preferred
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Highly organized and motivated individual with the ability to lead multiple projects and initiatives across diverse high performing matrix teams
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Possess excellent communication and presentation skills, both verbal and written
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He or she should understand pharmaceutical drug development including clinical development, regulatory, life cycle management of pharmaceutical products, and collaboration with Thought Leaders in the field
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The ideal candidate will have clinical expertise, and/or some relevant experience in the disease area within the pharmaceutical industry, such as within Medical Affairs or Clinical Development and in thoracic cancers
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Must have strong interpersonal and communication skills to navigate complex situations and gain alignment with diverse stakeholders, and work effectively within cross-functional teams
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Demonstrated ability to execute and deliver results in a deadline-driven environment while managing multiple priorities
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Estimated 25% travel (as applicable)
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If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Princeton - NJ - US: $166,350 - $201,571
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our careers site.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
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Health Coverage: Medical, pharmacy, dental, and vision care.
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Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
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Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
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US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
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Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information.
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
See All 43 Associate Director Medical Writing Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find JobsAssociate Director Medical Writing Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Associate Director Medical Writing Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
- Celgene Corporation10

- Juno Therapeutics10

- Eisai4

- Celgene3

- Insmed Incorporated3

Top Industries Hiring
- Biotechnology & Pharmaceuticals36
- Education2
- Animal Care & Pet Services1
- Distribution & Wholesale1
- Medical Devices1
What New Jersey Employers Look For
The qualifications that appear most often in associate director medical writing jobs across New Jersey.
- Advanced degree in life sciences, pharmacy, or a related scientific field
- Extensive experience authoring regulatory documents including CTDs, CSRs, and IBs
- Demonstrated experience managing or mentoring medical writers across projects
- Deep knowledge of ICH guidelines, FDA, and EMA submission requirements
- Strong cross-functional collaboration with clinical, regulatory, and biostatistics teams
- Experience with structured authoring tools and document management systems
Associate Director Medical Writing Jobs in New Jersey: Frequently Asked Questions
How many associate director medical writing jobs are there in New Jersey?
There are 43+ associate director medical writing openings in New Jersey on Migrate Mate as of June 2026, with the most roles in Princeton, Madison, and Nutley. New positions post regularly as employers across New Jersey hire.
Which New Jersey cities have the most associate director medical writing jobs?
Princeton, Madison, and Nutley have the most associate director medical writing openings in New Jersey right now, with additional roles spread across smaller metros statewide.
Which companies hire associate director medical writings in New Jersey?
Employers hiring associate director medical writings in New Jersey include Celgene Corporation, Juno Therapeutics, and Eisai, based on current listings on Migrate Mate as of June 2026.
Are there remote associate director medical writing jobs in New Jersey?
Yes. About 5% of associate director medical writing openings tied to New Jersey are remote or hybrid as of June 2026. The rest are on-site roles based in New Jersey metros.
How do I apply for associate director medical writing jobs in New Jersey?
You can apply to associate director medical writing jobs in New Jersey directly on Migrate Mate. Search the listings above, find roles that match your experience and preferred New Jersey location, then apply to each one that fits.
See All 43 Associate Director Medical Writing Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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