天津招聘

Key Accountabilities:

    

This position is expected to perform a leadership role in statistical programming and reporting areas, including but is not limited to the following:

• Ensure clinical trial data conforms with regulatory submission standards from CDISC, FDA, PMDA, China FDA, and other institutions.
• Document, archive and package clinical trial data, programs, and output as per SOP and regulatory requirements.
• Communicate proactively with stakeholders in data management, programming, statistics, and medical writing to provide high quality, timely, and efficiently-produced deliverables to clinical trial sponsors

                

Incumbents in this role receive highly competitive compensation and benefits. Highly driven, team-oriented, and quality-focused individuals have the potential to advance to technical or business leadership positions.

    

Tasks are performed in a timely, accurate, and efficient manner to ensure quality and productivity. In detail, the day to day tasks may include, but are not limited, to the following:

    

1. Develop SAS programs and generate complete, accurate and validated statistical outputs.

    

2. Program SDTM and ADaM datasets according to the dataset specifications.

    

3. Document data and programming information in accordance with Corporate Governing Documents (Policies, SOPs, or Work Instructions).

    

4. Archive clinical trial data (raw data, SDTM, and ADaM datasets) and programming documentation in accordance with Corporate Governing Documents and/or clinical trial sponsor’s specific requirements.

    

5. Manage programming assignments for project team members and follow up on task status to ensure deliverables are completed on time and with quality.

    

6. Provide training, mentorship, and technical guidance to less experienced Statistical Programmers or Biostatisticians who perform statistical programming.

    

    

Qualifications and Experience:

• A Master’s degree in Statistics, Biostatistics, Bioinformatics, Computer Sciences, and Mathematics, or other relevant fields is required with at least five years of relevant industry experience using SAS in clinical trial analysis and reporting. A College English Test (CET) 6 certificate is highly preferred.
• In-depth knowledge of clinical trial data processing and manipulation, hands on statistical programming and analysis.
• Knowledge of industry standards on how clinical trial data are structured, stored, analyzed, and presented to regulatory agencies.
• Knowledge of clinical trial regulatory, CDISC, and ICH requirements.
• Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies.
• Strong leadership skills and drive to achieve goals.

CGP 020是全球***家全面整合多行业的线上线下人力资源综合平台。

成立于2012年的CGP，脱胎于传统的猎头公司，拥有近400名专业人士为跨国公司与本土企业提供猎头、招聘流程外包和派遣服务，目前已成为亚洲***的提供招聘解决方案的公司之一。

公司在中国大陆有14个办公室，并在中国香港，新加坡和美国都设有办公室。

在2018年，公司大力发展线上的拥有强大AI匹配技术的招聘平台，并获得了多个业内奖项，包括***招聘机构和具创新能力招聘机构。

Human Resources Asia Recruitment Awards 2018
- ***招聘机构 - 最终大奖
- 具创新能力招聘机构 - 金奖

RI Asia 2017-2018
- 最具潜力招聘服务商
- 中国***招聘服务商

Top HR 2018
- 最具发展潜力本土猎头机构大奖
- 中国猎头行业排行榜内资 TOP 3