奖学金

这个为期两年的生物制造奖学金是与 教廷全球, FDA药品生产评估办公室(OPMA) 以及奥尔巴尼药学与健康科学学院. 

的 partnership of a global pharmaceutical company with a regulatory agency and an academic institution provides a rich and rewarding experience for the fellow. 除了, three partners build on their individual strengths and common objectives to create compelling projects over the two-year span.

的 fellowship is ideal for a PharmD and/or PhD holder who is interested in working in a dynamic environment with diverse cross-functional teams.

欲了解更多，请访问 教廷全球.

的 FDA药品生产评估办公室(OPMA) assures that quality pharmaceuticals are consistently manufactured over the product lifecycle. 欲了解更多信息，请访问 FDA药品生产评估办公室(OPMA).

最后期限:

• 提交申请的日期将在新的搜索开始之前列出

This fellowship will provide real-world experience and exposure to various functional areas within a Medical Affairs Department, 包括培训, 医疗信息, 以及医疗通讯, 在阿森迪斯制药公司为期两年的美国医疗事务奖学金项目期间, 专注于罕见疾病内分泌学.

这个混合型职位位于新泽西州普林斯顿. 该职位要求每周至少在现场工作两天.

主要职责 & 职责:

第一年学习目标:

• Obtain a comprehensive training within our disease states and products and/or investigational agent
• Develop scientific content for internal and external educational needs within Training and Medical Information, 包括现场资源和科学回应信.
• 研究 and anchor scientific content and participate in their review through the Medical and Promotional Review Committee process.
• 了解如何识别资源机会并评估供应商能力, 包括供应商选择, 预算计划和项目管理.
• 体验并参与产品发布的准备工作，以实现商业战略.
• Assist with onboarding and knowledge advancement activities for both field and internal Medical Affairs team members

第二年学习目标:

• Participate in planning and project pull-though for Training and other initiatives targeting Regional Medical Scientists (RMS/Medical Science Liaison -MSL) activities.
• 评估医疗信息查询并撰写标准回复信.
• 参加一次会议，参与展台覆盖，并审查响应指标.
• 全面了解良好的出版策划流程, 同时在出版物的战术执行中获得知识, 包括与外部作者合作撰写摘要, 海报展示, 以及用于平台演示的幻灯片, 以及为期刊出版物准备论文.
• Provide medical writing and editorial support for the scientific publication development process.
• 制作一份自我导向的出版物或海报，并在专业会议上展示.
• 描述从一开始临床试验设计的操作方面, 通过执行, 和收尾.

教育及经历:

• ACPE认证机构的药学博士学位.

知识、技能和能力:

• Excellent oral and written communication skills, ethics, professionalism, and leadership qualities
• 对科学有强烈的热情，对生物制药行业有兴趣
• Excellent time management skills with the ability to observe schedules and meet assignment deadlines
• 表现出积极的职业道德
• 具备独立工作和协同工作的能力

的 Innovate in 药物警戒 Fellowship is a post‐graduate training program designed to train pharmacists in pharmacovigilance, 提供研究和实地用药安全学习机会. 该项目提供为期两年的奖学金. 

药物警戒培训的新途径, 它于2021年启动，是药剂师之间的合作, 学术界的安全科学家和数据科学家, 工业和美国食品和药物管理局(FDA). 的 fellowship distributes training activities over a two‐year period including 12 months at a life sciences company; four months at ACPHS; and eight months at the FDA.

设计以药剂师的核心知识为基础, fellowship emphasizes three main areas of intensive training and competency development:

• 药物警戒
• 药物安全
• 数据科学

典型的活动包括安全监测和不良事件报告, 监测病人护理和用药系统的安全性和质量, 并对 FDA不良事件报告系统(FAERS)数据.

欲了解更多，请访问 BeiGene.

的 Crinetics Quality Assurance (QA) Fellowship provides two (2) years of comprehensive practical hands-on biopharmaceutical training and fosters an environment of learning within a fast-growing biopharmaceutical company.

同事与QA领导结对支持计划, 为各种临床试验和研究团队提供质量保证监督, 与各部门进行跨职能合作. 的 collaborative environment offers the fellow an enduring network and exposure to all aspects of the drug development process.

学习目标:

• 支持并参与GxP活动
• 开发跟踪关键绩效指标的工具, 创建KPI指标图表, 从记录和QA团队收集KPI数据.
• Track status and progress of the Annual Audit Schedule ensuring that audit deliverables are completed in a timely manner.
• 确保准确归档GxP审核记录, 调查报告, 相关的纠正和预防措施, 和偏差.  
• Assist in GxP Inspection Readiness Activities including the tracking and scheduling of Story Board development and reviews.
• 与QA团队一起确定供应商跟踪系统的改进, 认可供应商名单, 以及其他跟踪工具.
• 协助文档控制与格式, 编制和检讨电子数据管理系统内的受控程序.
• Work collaboratively with QA team to identify business processes and areas that require improvement and implement appropriate methods and tools to increase efficiencies.
• 支持EDMS系统管理员对系统配置更改进行用户测试.

申请材料:

• 意向书
• 两(2)封推荐信(LOR)，由每个推荐人直接通过电子邮件提交.
• 简历(CV)
• 非官方药学院成绩单
• Any additional materials that the candidate feels would be useful to the interview committee may be submitted.

最后期限:

• 提交申请的日期将在新的搜索开始之前列出.
• 面试将在申请审查后以滚动方式进行. 我们强烈鼓励尽早提交申请. 所有面试都将以虚拟方式进行.