
普通员工/个人贡献者
AI 估算 · 20k–30k
跨国药企上海办公室,硕士3年经验,出版岗位市场薪酬中等偏高,综合竞争力良好。
该职位负责制定并执行医学出版计划,确保发表物与公司战略及合规要求一致
Major in clinical medicine, science or pharmaceutical, master’s degree or above. 3+ years publication or related experience in pharmaceutical industry (either in pharmaceutical company or agency), CMPP prefer. In-depth understanding of clinical/medical affairs, scientific communication, publication, legal, regulatory requirement and governance management work.
Lead strategic publication planning and ensure high quality publication delivery in assigned therapeutic area. Publication Planning: Collaborate closely with medical, R&D and other relevant departments to develop annual publication plans and study publication plan with regular reviews and updates. Ensure publications are strategically aligned with the company's medical strategy, business objectives, and global publication strategy. Publication Management: Ensure strict adherence to compliance publication management processes; oversee the complete publication lifecycle including author invitation, manuscript review, author approval, journal selection and submission, and other key milestones to ensure compliance and timely publication delivery. Consultation Support: Proactively identify and resolve relevant issues, provide expert guidance on publication ethics and regulatory compliance to stakeholders. Vendor Management: Select and contract with publication medical writing providers; monitor and manage vendor performance in medical writing and manuscript development to ensure smooth publication preparation processes and quality deliverables. Deploy multichannel medical communication to maximize the impact of relevant evidence communications. Lead post-publication data dissemination activities, including developing newsletter templates, tracking internal communications, and managing medical material approval processes. Assist in developing internal communication materials to support effective dissemination of research progress and key scientific updates across the organization. Participate in the execution of multichannel medical communication strategies. Proactively seek innovative medical communications solutions for critical business needs. Cross-Functional Collaboration, serves as a partner in medical communications, establishing deep glocal collaborative relationships with teams across medical, R&D, HEVA, legal, compliance, and regulatory functions at both glocal and regional levels. Develop or review medical communication clauses in study/Research or project contracts to ensure compliance with company policies. Develop comprehensive monitoring strategy to keep updated on proceedings in assigned therapeutic area and provides up-to-date scientific information and intelligence report to Medical and other relevant team. Oversee and manage HGRAC compliance for scientific publications, including policy monitoring, workflow coordination, and documentation management. Ensure all communication materials and activities are conducted with due regard to all applicable local, regional, global, and national laws, regulations, guidelines, codes of conduct, company policies, and accepted standards of best practice.
Publication experience as physician in hospital preferred. Experience in the pharmaceutical as medical manager, medical liaison or other R&D/Medical related functions preferred. Proven success at leading or managing medical communications agencies or projects preferred.
优点
缺点 / 挑战
跨国药企出版专家岗,专业性强、社会价值高,但办公灵活性一般。
跨国药企全职岗位,薪资有竞争力且福利完善,但JD未明确数字,需面议。
职位提供深度出版和医学传播经验,有跨部门协作和项目管理成长机会,但未提及晋升通道。
仅现场办公,工作地点在上海市区(未明确),JD未提及弹性工作或WLB,推测为正常办公强度。
制药行业致力于改善患者健康,职位推动科学证据传播,有明确社会价值。