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Regeneron Pharmaceuticals, Inc (USA)
Director, Publications
Career Insights for Corporate Development Manager
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What they do
A Corporate Development Manager helps develop, manage and analyze corporate development through mergers and acquisitions or strategic alliances. Leads research, cost/benefit analyses of mergers, and communicates results to stakeholders. Includes developing and maintaining professional relationships, marketing the proposed changes and assisting in transitions.
$163,559 / year median in New York
+3% projected growth
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 a Director, Publications, to join our Medical Affairs team, supporting cross-functional and alliance-wide publication strategy for assigned therapeutic assets. In this role, you will lead the strategic direction and operational performance of publication plans while collaborating with authors, Medical Affairs partners, cross-functional collaborators, and external agency partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where:
Location:
Sleepy Hollow, NY or Warren, NJ Work model/flexibility: On-site 4 days/week. If based in Warren, NJ, travel to Sleepy Hollow will be expected. Discover your role :- Lead and accountable for cross-functional and alliance-wide publications teams.
- Lead publications review of annual plans and projects with senior management
- Lead in defining and building consensus on terms for literature and gap analyses to support scientific communication platform development and publication strategy
- Pub plan and medical communication strategy development and evolution
- Partner with procurement for agency selection and agency performance management
- Budget accountability for agency external resource scope of work (SOW) development, budget tracking, and invoicing according to approved SOW/PO, reflecting work completed
- Manage writers/agencies for individual pubs projects to effectively complete execution within specified timelines
- Responsibility for alignment on scientific content/communication objectives, author invitations, collection of author agreements, securing medical/clinical lead materials for kick-off meeting discussions, author kick-off calls
- Review assigned publications ensuring quality, alignment with scientific communication platform, and compliance with standards for ethical reporting of study data
- Oversee efficient and compliant financial management
- Ensure adherence to established compliance, regulatory, and ethical standards across all publication activities, including disclosure requirements, TOV guidelines, billing practices, and review documentation
- Proactively identify and communicate operational risks, delays, or issues
- Working with Executive Director, Publications identify and lead meaningful process improvements and innovations initiatives, as appropriate based on business needs This role requires:
- Doctorate scientific degree required (PhD, PharmD, or MD) along with 7+ years of experience in medical communications or publications management within the pharmaceutical or biotechnology industry
- Minimum 3 years of experience independently leading cross-functional, therapeutic area-specific publication plans
- Proven track record managing complex, multi-asset publication plans, ideally within Oncology, Ophthalmology, Hematology, or Rare Diseases
- Experience managing external agency partners and publication vendors, including budget oversight and SOW management Does this sound like you?