生物统计学高级经理,生物相似药
Biostatistics Senior Manager, Biosimilars
### **职业类别**
医学事务
### **职位描述**
### 加入安进,为患者服务
在安进,如果你觉得自己是更大事业的一部分,那是因为你确实是。我们的共同使命是帮助患有严重疾病的患者,这推动着我们所做的每一件事。
自1980年以来,我们在对抗世界上最难治愈的疾病方面,帮助开创了生物技术的世界。我们专注于四个治疗领域——肿瘤学、炎症、普通医学和罕见病,每年惠及数百万患者。安进正在推进广泛的药物管线,用于治疗癌症、心脏病、炎症性疾病、罕见病以及肥胖及其相关疾病。作为安进团队的一员,你将帮助对患者的生活产生持久影响,我们通过研究、生产和交付创新药物,帮助人们活得更长、更充实、更快乐。
我们获奖的文化是协作、创新和基于科学的。如果你热衷于挑战,并且能在其中找到机会,你将在安进团队中茁壮成长。加入我们,改变患者的生命,同时改变你的职业生涯。
生物统计高级经理,生物类似药美国-远程办公
让我们一起行动,改变世界。在这个关键角色中,你将领导一个大型产品,或更复杂的试验和/或项目,确保所有与临床活动相关的文件的统计方面符合要求并具有统计准确性,影响并参与发展战略,并在内部和外部捍卫统计方法。
**职责**
- 实施、监督并支持策略、研究设计和统计分析中的标准、技术质量和一致方法。
- 计划并执行对方案、随机化规范、统计分析计划(SAP)、表、列表和图形(TLG)模板、提交数据文件(SDF)规范、其他关键研究相关文档、方案偏离、快速备忘录、临床研究报告(CSRs)和其他沟通内容的统计贡献,与CRO在全服务CRO模式下紧密合作。
- 为临床出版物、临床安全性摘要(CSSs)、临床有效性摘要(CSEs)、临床概览(COs)和监管文件提供统计输入。
- 监督在全服务CRO模式下由CRO进行的统计工作。
- 执行多中心试验的统计分析
查看英文原文
### **Career Category**
Medical Affairs
### **Job Description**
### Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Biostatistics Senior Manager, Biosimilars US- Remote
Let’s do this. Let’s change the world. In this vital role you will lead a single large product, and/or more complex studies and/or projects, ensures that all statistical aspects of documentation pertaining to clinical activities meet required standards and are statistically correct, influences and contributes to the development strategy, and defends statistical approaches internally and externally.
**Responsibilities**
- Implements, oversees and supports standards, technical quality and consistent approaches in strategy, study design and statistical analysis.
- Plans and executes statistical contributions to protocols, randomization specifications, Statistical Analysis Plans (SAPs), Table, Listing and Graph ( TLG) shells, Submission Data File (SDF) specifications, other key-study related documentation, protocol deviations, Flash Memos, Clinical Study Reports (CSRs), and other communications in close partnership with CROs in a full-service CRO model.
- Provides statistical inputs to clinical publications, Clinical Summary of Safety (CSSs), Clinical Summary of Efficacy (CSEs), Clinical Overviews (COs), and regulatory documents.
- Oversees statistical work performed by CROs in a full-service CRO model.
- Performs statistical analysis of multiple studies/projects and subsequent exploratory analyses, and makes sound conclusions and recommendations.
- Represents the Biostatistics function and participates in multidisciplinary project team meetings; collaborates closely with other functional team members; incorporates knowledge of cross-functional areas to inform and provide sound statistical guidance to teams (e.g. provides support and input in case report form design, and data collection).
- Proactively anticipates and communicates resource and quality issues that may impact deliverables or timelines within functional area as well as cross-functionally.
- Be familiar with statistical policy and strategy at Amgen; having working knowledge of theoretical and applied statistics and of regulatory guidelines and industry practice on biosimilar development.
- Stays abreast of latest developments in the field of statistics in drug development and contributes to scientific advances by publishing applied research in scientific journals and books and presenting statistical methodology at internal or external scientific meetings.
- Participates in the review of CRO Policies, SOPs and other controlled document development, and in the development and review of Amgen-CRO’s process maps; contributes to process improvement and operational efficiency.
- Adheres to all Amgen Policies, Standard operation procedures (SOPs) and other standards which are applicable to biosimilar development.
### **What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a Biostatistics Senior Manager, with these qualifications.
**Basic Qualifications**
- Doctorate degree and 2 years of Biostatistics experience
OR
- Master’s degree and 6 years of Biostatistics experience
OR
- Bachelor’s degree and 8 years of Biostatistics experience
**Preferred Qualifications**
- Masters degree in Statistics/Biostatistics or other subject with high statistical content, and 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research
Or
- Doctoral degree in Statistics/Biostatistics or other subject with high statistical content, and 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research
- Knowledge/experience of biosimilars development, non-inferiority or equivalence trials
- Statistical contributions to regulatory submissions
- Experience in statistical methodologies related to adaptive designs (e.g., group sequential design, adaptations to treatment arm selection design, Bayesian adaptive design) and/or combined phase 1/2 or phase 2/3 design
- Independent leadership of the design, analysis and reporting of at least 1 complex or multiple less complex studies/projects within the Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia
- Demonstrated ability to provide sound strategic and statistical input on study/research design to meet project needs, regulatory and scientific requirements
- Demonstrated ability in presenting results and defending statistical findings, study design and analysis. This could be to internal audiences (study/product team) **or** at external meetings such as investigator meetings, steering committee meetings, ad board meetings or regulatory meetings
- Demonstrated ability in working within a global team and with CRO partners to ensure operational excellence and efficiencies
- Demonstrated effective communication skills (written and oral)
### **What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
### Apply now and make a lasting impact with the Amgen team.
### **careers.amgen.com**
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
### Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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**Salary Range**
154,104.15USD -208,493.85 USD