天津招聘

职位描述：
Position Title: Senior Manager of SAS Programming
Department: Statistics / SAS Programming
JOB PURPOSE

Summarizes the job’s purpose or role and why it exists in the organization
SAS Programming Team in the department of Statistics of Hengrui R&D Center provides clinical programming support for various clinical studies and contributes to the development of departmental standards. Senior Manager of SAS Programming is accountable for programming team deliverables for the assigned clinical projects. This role is that of a programming lead who plans and provides oversight of SAS programming activities (e.g., development, verification and documentation) in support of clinical trial reporting and submissions.

NATURE & SCOPE

a) Organization Structure
Report to: Head of Statistical Programming
Number of Subordinates: TBD
b) Key Working Relations
Communicates with statistician and medical manager to fully understand analysis requirements for assigned clinical projects, leads the programming team to perform all SAS programming tasks with high quality in the agreed timeline, and works closely with data management to assure data quality, sometimes needs to interact with project/study manager on periodic trial management reports.

JOB REQUIREMENTS
Academic / Professional Qualification
- Minimum of a Bachelor’s degree in Statistics, Mathematics, Computer Science, Pharmaceuticals Sciences, Life Sciences, Public Health or other related areas. Master's Degree is preferred.
- In-depth knowledge of SAS programming, statistics, clinical drug development process and regulatory requirements related to the role.

Technical / Skills Training
- In-depth knowledge of Base SAS, SAS/STAT, SAS Graph, SAS SQL and SAS Macro Language. SAS Certification is preferred, not required.
- Basic knowledge to use Windows Operating System, and Microsoft Office (Word, Excel, PowerPoint and Outlook). Knowledge of Visual Basic, Java, Python or Perl programming language is preferred.
- Effective communication skills and ability to establish and maintain effective working relationships with study team members. Being fluent in spoken and written English.
- Thorough understanding of relational database components and theory.
- Solid analytical and problem solving skills paired with strong attention to detail.
- Must be a motivated, self-directed learner with a passion and drive for technology.
- Ability to work under pressure and manage multiple projects simultaneously.


Working Experience
- Minimum of 7 years of proven experience in SAS programming. Pharmaceutical/Clinical trial experience is required.
- Must have at least 2 years of experience of mentoring junior programmers.
- In-depth knowledge of analysis requirements for endpoints in multiple therapeutic areas (TAs), oncology TA experience is highly desirable.
- Experience working with external vendors/CROs is desired.
- Knowledge of relevant internal and external standards and guidance for clinical development (CDISC, EMEA/FDA, ICH-GCP etc.)
- Fully accountable for the programming work.

DUTIES & RESPONSIBILITES
Key Tasks
- Participates in review of protocol, statistical analysis plan (SAP), data integrity plan (DIP), data management plan (DMP) and case report form (CRF).
- Participates in creation of programming documents including list of tables, mock tables, analysis specifications, dataset specifications and other related documents, and ensures all programming-related files are in the appropriate location on the company server.
- Is accountable for the production of high-quality, on-time statistical programming deliverables (such as datasets and tables/listings/figures (TLFs)) for either outsourced or insourced clinical studies and development programs.
- Works with data management to perform data quality checks.
- Ensures clear and timely communications with study team members.
- Ensures all programming activities following regulatory requirements and company SOPs.
- Mentors new hires or provide training to SAS programmers.
- Participates in the development and implementation of programming tools for data analysis and reporting.
- Contributes to development of programming related SOPs.
- Provides regular oversight of statistical programming work outsourced to programming vendors/CROs and acts as a liaison between the vendor/CRO and the Hengrui Biostatistics and Programming function. 举报 分享

上海恒瑞医药有限公司系江苏恒瑞医药股份有限公司的全资子公司，注册资本7200万元，前期建设投资1.8亿元。公司设位于上海闵行经济技术开发区内，其中研发中心占地10053.53平方米，于2004年5月投入使用。在科研开发方面，公司将瞄准国际先进水平，建立科研基础平台，积极拓展新药研发领域，增加产品剂型，填补国内空白，参与国内国际市场竞争，提高民族医药工业水平。整个研发中心致力于创新药物的发现，以极大的热情向社会提供以科研开发为基础，适合市场需求的高科技医药产品。

为什么要选择上海恒瑞？为什么上海恒瑞一定成功？

***，我们拥有雄厚的资本，决意发明新药，并且已作巨额投资；第二，我们已有丰富的临床和市场发展经验，从实验发明到投入市场的时间大量减少；第三，有能力从目标化合物设计合成，体外体内筛选，药代毒理，药理到GMP生产完全自办；第四，我们拥有一支经验丰富的新药发展团队，融入其中的每位员工都可以增加新药发明过程的经验；第五，我们聘请***的人才，采用先进的生物工程管理方法，以工作表现为基础的薪金奖金制度、活动工作时间以及无上限研究级别升级；第六，我们拥有先进的实验设施—无任务上限的Scifinder的化学信息库等，我们拥有绝对无烟的工作环境，而且先进的实验设备也为我们创造了一个无噪音、无气味的健康环境；第七，我们从事的是真正的有知识产权的新药研发，而不是生产中间体。

Discovering drugs not making intermediates

Shanghai Hengrui Pharmaceuticals Co. Ltd. is a fully integrated drug discovery company with marketed products well funded by a top Chinese pharmaceutical company dedicated to discovery of IP protected New Chemical Entities (NCEs). We are conveniently located in Minhang Economic Zone, 30 minutes from the vibrant Shanghai downtown and occupy a new 10,000 square meter. laboratories equipped with state-of-art instruments. We are currently recruiting scientists in all areas of drug discovery.

We offer a locally competitive compensation and benefits package and provide a highly interactive, open, challenging, smoke-free and campus-like environment. We have also adopted a performance based award system and created a scientific ladder for dedicated and motivated individuals to grow within the company. If you are interested in joining this new drug discovery revolution in China, please forward your resume to Miss Hong (career@shhrp.com) for immediate consideration. Applicants from other areas of drug discovery are also invited to send in their CVs.