Associate Director, Publications

BioSpace; Village of Sleepy Hollow (NY); On-site; USD 157,000 - 257,000; Full time

Benefits offered by this job

Relocation benefits

Job summary

Regeneron is seeking an Associate Director, Publications to lead dissemination plans across clinical, HEOR/RWE, PKPD, and disease-state publications. You will collaborate with cross-functional teams and alliance partners to ensure research is communicated accurately and on time.

This role requires shaping the narrative, guiding publication teams, managing budgets, and reporting metrics. On-site work in Warren, NJ or Sleepy Hollow, NY is required with relocation benefits available.

Qualifications

• Advanced degree in science with relevant publications experience.
• Excellent writing and editing capabilities.
• Familiarity with GPP 22, ICMJE, OIG, PhRMA, Sunshine Act, copyright guidelines.
• Experience leading multi-disciplinary and alliance-based publication teams.

Responsibilities

• Lead development of scientific, clinical, and health-outcomes publications, ensuring accuracy and timely delivery.
• Shape the scientific narrative and lexicon behind data, translating findings into clear strategic communication.
• Guide cross-functional and alliance publication teams through collaboration and alignment.
• Oversee budget, forecasting, and resource allocation, tracking expenditures.
• Identify gaps and opportunities to evolve the publication strategy.
• Report post-publication metrics and maintain records in Publication Management Tool.
• Manage timelines, quality, and efficiency across publication activities.
• Review manuscripts, abstracts, and presentations with cross-functional colleagues.

Skills

Publication writing

Editing skills

Regulatory guidelines

Cross-functional collaboration

Education

Master's degree in science

PhD/PharmD/MD

Job description

Build Our Future Together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Publications to lead the development and execution of aligned dissemination plans across clinical, HEOR/RWE, PKPD, and disease state publications, while collaborating with cross-functional teams, alliance partners, and leading medical and scientific experts to ensure our research reaches the community accurately and on time.

Build Our Future Together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Publications to lead the development and execution of aligned dissemination plans across clinical, HEOR/RWE, PKPD, and disease state publications, while collaborating with cross-functional teams, alliance partners, and leading medical and scientific experts to ensure our research reaches the community accurately and on time. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & Where Location: Warren, NJ or Sleepy Hollow, NY Work model/flexibility: On-site, 4 days/week (relocation benefits available if eligible; hybrid or fully remote not offered)

Discover Your Role

• Lead the development of scientific, clinical, and health-outcomes publications, ensuring accuracy, readability, and timely delivery
• Shape the scientific narrative and lexicon behind our data, translating statistical findings into clear strategic communication
• Guide cross-functional and alliance-wide publication teams through collaborative discussion, independent research, and strategic alignment
• Oversee budget, forecasting, and resource allocation, tracking expenditures and flagging issues early
• Partner across functions to identify gaps and opportunities that continually evolve our publication strategy
• Accurate and timely reporting of post-publications metrics, compliant maintenance of records in the Publication Management Tool (e.g., iEnvision), vendor and budget management.
• Manage timelines, quality, and efficiency across publication activities
• Track and report post-publication metrics, maintaining compliant, well-documented records
• Review and submit manuscripts, abstracts, and presentations in partnership with cross-functional colleagues

This Role Requires

• Master's degree in science with 8+ years of related experience, or PhD/PharmD/MD with 5+ years of experience in medical affairs, publications, or scientific communications
• Strong publication, writing, and editing skills
• Working knowledge of Good Publication Practice (GPP 22), ICMJE, OIG, PhRMA code, Sunshine Act, and copyright/permission guidelines
• Experience collaborating within multi-disciplinary teams and alliances with drug development partners

Oncology, Ophthalmology Or Hematology Experience Preferred

We are committed to building a workplace with an inclusive culture.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$157,200.00 - $256,600.00