- 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
- 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
- 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
- Post-graduate degree in Pharmaceutical Science or graduate in Medical science (MBBS)
- Prior 4 to 5 years work experience as a member of Promotional and more medical/ scientific material review team
- Demonstrated lightspeed operational excellence experience
- Ability to manage multiple projects and timeframes in complex organizational structure
- Able to interact, partner and provide thought leadership for key stakeholders with comfort and ease
- Experience working with agencies/vendors
- Acts decisively in complex and fast-moving environment
- 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 English and strong functional fluency in spoken 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/ Zinc/ PMAW) is required.
-
Novo Nordisk A/S Hangzhou, 中国您在寻找一家专注于行业并且以患者为中心的公司吗? 您准备好加入我们有竞争力的团队了吗?诺大世界,和您同行 · 职位介绍 · 通过RDPAC考试认证 · 带领团队做好市场拓展,包括开发新的医疗机构,新的科室客户,新的渠道,商业模式的拓展。 · 负责带领所辖区域团队完成所管辖区域的销售目标,做好与销售有关的活动; · 建立一支有凝聚力、有竞争力的"高绩效、高合规"的销售队伍; · 在所辖区域推动跨部门的合作,以加速药物可及性,并且赢得市场竞争; · 塑造肥胖症这个新的疾病领域,并协助客户做好肥胖症诊疗的高质量长期发展规划。 · 持续寻找机会增长点,满足更 ...
-
Bosch Hangzhou, 中国 全职Job Description · Lead the cross-functional project team follow the Bosch product development process and complete the project according to the agreed targets/goals. · Organize discussions, formulate project plan and project goals, lead the project team to follow the project plan ...
Content Reviewer医学内容审核专员 - Hangzhou, 中国 - Pfizer
描述
Job Summary:
The Content Reviewer will be responsible for regular operational review of promotional, regulatory, training and continuing medical education material in compliance with relevant SOPs/ regulations / industry codes/ working practices, mainly online contents produced from content factory.
Success will be met through exceptionally close coordination and partnership within Customer Innovation Operation team, with Medical Affairs, Medical Information, Medical Quality Governance, Compliance, Content Enablement, etc.
Responsibilities:
Education and Experience:
Technical Skills Requirements:
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical#LI-PFE
