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Associate Medical Reviewer
10-15K/月广东省-广州/硕士及以上/1-3年
麦婉琪今天来过
辉瑞投资有限公司
职位详情
岗位职责
Job Purpose
Responsible for supporting the Pfizer Research & Development group Medical Information and Review, specifically:
· Working collaboratively with Medical and Marketing teams to review promotional, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
· Advocating best practices for achieving effective and complaint medical and promotional communications for Pfizer products
· Under supervision from line manager, ensuring that the operational deliverables of assigned deliverables are achieved on or ahead of schedule and within standards such that they meet the desired outcomes (i.e. quality standard, value)
Main Responsibilities
1. Technical
• Uses scientific expertise and medical knowledge to ensure appropriate review of promotional, regulatory, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
• Liaises with all commercial functions in the review for scientific/ medical accuracy prior to and through the MLR review process as required
• Ensuring clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
• Collaborating with other lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned documents
• Assists in generating and reviewing any additional support content, including proof reading, reviewing, referencing and verifying anti-plagiarism of the content
2. Tactical/ Operational
• Maintains the promotional material review process and system knowledge as per Pfizer standards
• Produces analytics reports and project scorecards as required in line with decided KPIs and sharing these with the line manager
• Monitors miletones, idententifing potential risks and assisting in resolving any issues
• Assists in coordinating activities of other team members to ensure the quality and accuracy of their contributions
• Conducts quality control assessments of assigned deliverables as required
3. Project Planning, Execution and Delivery
• Prioritizes and multitasks to enhance productivity and manage workload
• Under supervision from line manager, communicates with stakeholders regarding project progress to cross functional teams and ensuring that quality standards are being met and to optimize efficiency
• Delivers assigned documents on or before deadline, alerting project teams in a timely manner of any anticipated delays, information gaps or potential shortcomings in quality
Others
1. Mentorship – actively mentors other team members for effectice execution of assigned tasks and goals
2. Keeps abreast of current literature, emerging science, technological developments and medical trends for enhancing content review and development
3. Values and Behaviors - Consistently adheres to/demonstrates all Pfizer values, with special focus on integrity, performance and teamwork. Works in harmony with internal and external stakeholders
4. Personal Development - Enhances self-development through on-the-job training. In consultation with line manager, identifies additional areas of interest towards learning and development, along with training needs and gaps.
5. Performance Management System (PMS) – Ensures full compliance to PMS
Qualification & Experience
• Post-graduate degree in Pharmaceutical Science or graduate in Medical science (MBBS)
• Prior work experience as a member of Promotional and more medical/ scientific material review team
Special Skills & Knowledge
• Technical skills: Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant Therapeutic Area/Products
• Writing skills: Excellent writing skills
• Analytic skills: Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them. Analytical skills and reasoning, and sound medical judgment/decision making
• Language skill: High fluency in written Cantonese/English and strong functional fluency in spoken Cantonese/English.
• Personal skills. Strong organizational skills and ability to prioritize multiple projects and meet deadlines.
• Interpersonal skills: Effective influencing and negotiating skills, including when appropriate an ability to guide decision-making for document content strategy. Ability to work well with all levels and roles in cross-functional, global teams.
• Regulatory knowledge: Familiarity with global regulatory guidance (especially ICH, FDA and EMA) relevant to clinical and safety data.
• Software: Previous experience with software commonly used to present and analyze data and experience with searching academic databases.(Word, PowerPoint, Excel) is preferred. Working knowledge of tools to aid the promotional material review process (GCMA) is required.
Responsible for supporting the Pfizer Research & Development group Medical Information and Review, specifically:
· Working collaboratively with Medical and Marketing teams to review promotional, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
· Advocating best practices for achieving effective and complaint medical and promotional communications for Pfizer products
· Under supervision from line manager, ensuring that the operational deliverables of assigned deliverables are achieved on or ahead of schedule and within standards such that they meet the desired outcomes (i.e. quality standard, value)
Main Responsibilities
1. Technical
• Uses scientific expertise and medical knowledge to ensure appropriate review of promotional, regulatory, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
• Liaises with all commercial functions in the review for scientific/ medical accuracy prior to and through the MLR review process as required
• Ensuring clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
• Collaborating with other lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned documents
• Assists in generating and reviewing any additional support content, including proof reading, reviewing, referencing and verifying anti-plagiarism of the content
2. Tactical/ Operational
• Maintains the promotional material review process and system knowledge as per Pfizer standards
• Produces analytics reports and project scorecards as required in line with decided KPIs and sharing these with the line manager
• Monitors miletones, idententifing potential risks and assisting in resolving any issues
• Assists in coordinating activities of other team members to ensure the quality and accuracy of their contributions
• Conducts quality control assessments of assigned deliverables as required
3. Project Planning, Execution and Delivery
• Prioritizes and multitasks to enhance productivity and manage workload
• Under supervision from line manager, communicates with stakeholders regarding project progress to cross functional teams and ensuring that quality standards are being met and to optimize efficiency
• Delivers assigned documents on or before deadline, alerting project teams in a timely manner of any anticipated delays, information gaps or potential shortcomings in quality
Others
1. Mentorship – actively mentors other team members for effectice execution of assigned tasks and goals
2. Keeps abreast of current literature, emerging science, technological developments and medical trends for enhancing content review and development
3. Values and Behaviors - Consistently adheres to/demonstrates all Pfizer values, with special focus on integrity, performance and teamwork. Works in harmony with internal and external stakeholders
4. Personal Development - Enhances self-development through on-the-job training. In consultation with line manager, identifies additional areas of interest towards learning and development, along with training needs and gaps.
5. Performance Management System (PMS) – Ensures full compliance to PMS
Qualification & Experience
• Post-graduate degree in Pharmaceutical Science or graduate in Medical science (MBBS)
• Prior work experience as a member of Promotional and more medical/ scientific material review team
Special Skills & Knowledge
• Technical skills: Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant Therapeutic Area/Products
• Writing skills: Excellent writing skills
• Analytic skills: Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them. Analytical skills and reasoning, and sound medical judgment/decision making
• Language skill: High fluency in written Cantonese/English and strong functional fluency in spoken Cantonese/English.
• Personal skills. Strong organizational skills and ability to prioritize multiple projects and meet deadlines.
• Interpersonal skills: Effective influencing and negotiating skills, including when appropriate an ability to guide decision-making for document content strategy. Ability to work well with all levels and roles in cross-functional, global teams.
• Regulatory knowledge: Familiarity with global regulatory guidance (especially ICH, FDA and EMA) relevant to clinical and safety data.
• Software: Previous experience with software commonly used to present and analyze data and experience with searching academic databases.(Word, PowerPoint, Excel) is preferred. Working knowledge of tools to aid the promotional material review process (GCMA) is required.
任职要求
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公司信息
辉瑞投资有限公司
- 上海
- 1000-9999人
- 生物技术
- 外企
- 不需要融资
辉瑞公司（Pfizer Inc.）创建于1849年，总部位于美国纽约，是一家以科学为基础的、创新的、以患者为先的生物制药公司。辉瑞的使命是“为患者带来改变其生活的突破创新”。
在辉瑞，我们通过科学和全球资源为人们提供治疗方案，以延长其生命，显著改善其生活。在医疗卫生产品的探索、研发和生产过程中，辉瑞始终致力于奉行严格的质量、安全和价值标准。
我们在全球的产品组合包括创新药品和疫苗。每天，辉瑞在发达和新兴市场的员工都在推进人类健康，推动疾病的预防、治疗和治愈，以应对挑战我们这个时代的顽疾。
辉瑞还与医疗卫生服务方、政府和社区合作，支持并促进世界各地的人们能够获得更为可靠和可承付的医疗卫生服务。这与辉瑞作为一家全球卓越的创新生物制药公司的责任是一致的。170余年来，辉瑞一直致力于为所有依赖我们的人带来改变。
辉瑞于1989年进入中国市场。扎根中国30余年，辉瑞已成为在华主要的外资制药公司之一。2021年是辉瑞新征程的开始。迄今已有170余年历史的辉瑞正在迈入全新时代，成为一家以科学为基础的、创新的、以患者为先的生物制药公司。目前辉瑞在中国业务覆盖全国300余个城市，累计投资超过15亿美元，并设立了1家先进的生产设施，2个研发中心（分别位于上海张江高科技园区和武汉光谷），在华有近7,000名员工分布于业务、研发和生产等领域。辉瑞在华上市了五大领域的高品质创新产品，包括肿瘤、疫苗、抗感染、炎症与免疫、罕见病等多个领域的处方药和疫苗，强大完善的产品线旨在满足生命各阶段的健康需求。
多年来，辉瑞始终致力于“成为中国医疗卫生体系重要组成部分”，运用全球医疗资源，与社会各界合作，积极推进中国健康事业。未来，辉瑞将继续践行“为患者带来改变其生活的突破创新”的使命，秉承“科学致胜”的理念，以创新为动能，与中国政府部门和社会各界合作，积极引进突破性的创新药物，探索药物可及性创新方案，及时惠及中国患者，助力“健康中国2030”宏伟目标的实现！
