2 часа назад
Senior Publications Manager (Scientific Publications)
121 050 - 211 840$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Publications Manager (Scientific Publications): Executing compliant scientific publication plans across pharmaceutical therapies, coordinating authors, agencies, reviewers, journals, and congresses with an accent on publication planning, project governance, and medical communications. Focus on managing manuscripts and publication assets, tracking budgets and timelines, applying GPP and ICMJE standards, and maintaining inspection-ready systems and records.
Location: Plainsboro, New Jersey, United States; 10–20% overnight travel required.
Base compensation: $121,050–$211,840 per year, plus potential bonus and long-term incentive compensation.
Company
develops healthcare solutions focused on serious chronic diseases and improving long-term patient health.
What you will do
- Execute approved publication plans across assigned therapies and therapeutic areas.
- Coordinate authors, agencies, journals, congresses, internal reviewers, and cross-functional stakeholders.
- Manage manuscripts, abstracts, posters, oral presentations, author meetings, submissions, approvals, and publication records.
- Track project timelines, dependencies, budgets, vendor deliverables, risks, metrics, and corrective actions.
- Apply GPP 2022, ICMJE, company SOPs, external publication guidelines, and compliance requirements.
- Provide workflow guidance and training while maintaining accurate, inspection-ready publication and author-engagement systems.
Requirements
- MS, MD, PhD in Life Sciences, or PharmD required.
- At least 3 years of relevant experience in pharma, biotech, or a medical communications agency, including scientific publication projects.
- Experience coordinating, preparing, reviewing, and submitting scientific publications in multiple formats.
- Proficiency with publication management and author-engagement systems, document workflows, Microsoft Office, and approved digital or AI tools.
- Strong project management, organizational, written communication, and stakeholder relationship skills.
- Ability to work independently and in multidisciplinary teams, with 10–20% overnight travel required.
Nice to have
- CMPP certification.
- Knowledge of diabetes, obesity, and rare disease therapeutic areas.
Culture & Benefits
- Patient-centered, collaborative work across Medical Affairs, Clinical Development, Biostatistics, HEOR/RWE, Regulatory, Legal/Compliance, Market Access, and Marketing.
- Medical, dental, vision, life, disability, and flexible spending benefits.
- 401(k) savings plan, tuition reimbursement, employee assistance, and voluntary insurance programs.
- Sick time, flexible vacation, and parental leave policies.
- Inclusive recruitment and equal employment opportunity commitment.
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