上海招聘高级统计分析员/Senior Statistical Programmer

高级统计分析员/Senior Statistical Programmer

美斯达（上海）医药开发有限公司

公司规模：150-500人
公司性质：外资(欧美)
公司行业：制药/生物工程

职位信息

发布日期：2017-01-13
工作地点：上海-闵行区
招聘人数：若干人
职位月薪：10000-14999/月
职位类别：临床数据分析员

职位描述

职位描述：

POSITION SUMMARY:

Responsible for the planning, development, quality control and documentation of statistical programs in support of department projects.

PRINCIPAL RESPONSIBILITIES:

1.Deliver individual programming deliverables of projects with medium to high complexity.

2.Perform quality control in support of clinical trial activities.

3.Plan and develop programs to produce tables, listings, figures and other reports and analyses summarizing clinical trial results.

4.Plan and develop programs to produce electronic submission deliverables.

5.Maintain documentation as appropriate.

6.Assist in the review and input into project requirements.

7.Participate in clinical project team meetings as required.

8.Mentoring, training of junior programmers.

9.Demonstrate full proficiency in technical/programming skill

PRINCIPAL RELATIONSHIPS:

Contacts: Programming; Biostatistics; Data Management; Clinical Pharmacology; Medical Writing; Quality Management; other related working groups

EDUCATION AND EXPERIENCE REQUIREMENTS:

Master’s degree in computer science, mathematics, health statistics or other scientific field +2-3 years’ experience or Bachelor’s degree in computer science, mathematics, health statistics or other scientific field + 4-6 years’ experience programming and analyzing scientific data in pharmaceutical or biotechnology industry.

Very strong knowledge of SAS programming and/or other statistical software (e.g., S-Plus, R, PASS).

Good communication skills in written and oral English.

职能类别：临床数据分析员

关键字：统计程序员统计分析员

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公司介绍

美斯达（上海）医药开发有限公司于2005年11月成立，是一家合同研究组织（Contract Research Organization，简称CRO），提供专业化的临床试验（Clinical Trail）数据管理（Data Management）、统计分析（Statistical Analysis）和试验报告撰写等服务。美斯达在临床试验领域提供的服务包括: 临床试验方案设计，数据库设计和创建，病例报告表设计，数据管理，撰写统计分析计划（SAP），创建分析数据集，用SAS程序进行统计学分析，制作统计表，统计图及数据列表，对新药综合疗效（ISE）及安全性（ISS）报告进行统计分析，撰写独立的统计学报告以及注册申报用的临床试验报告，出席美国或中国的药政机构审评会，回答数据统计问题，支持药品注册申报。公司具有丰富的医药及临床试验经验，尤其擅长下述治疗领域的临床试验数据管理和分析: 疼痛、癌症、心血管、呼吸系统、中枢神经系统、抗病毒，抗生素、和消化系统等。

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