Data Manager

Parexel International Pesquisas Clinicas LTDA.

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China-Shanghai Shinmay Until 8/21/2026 5+ years exp H-1B sponsor history First posted June 22, 2026 Last posted June 22, 2026
Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

(a) Key working relationships / 主 要 工 作 关 系
- Internal contacts within AZ / 内 部 联 系
• Clinical Research Team
• Quality Assurance / Quality Control
• Local drug supply chain
• R&D, GMA, Global ESRO, etc
• Procurement
• Regulatory Affairs
- External contacts with organizations outside AZ / 外 界 联 系
• Principal Investigator/Co-Investigators
• CRO/SMO
• Any other vendors if related to function scope and responsibility
(b) Job requirements /工 作 要 求
• Results Driven Behavior
• Self-motivation and adaptability
• History of successful managerial experience on project management
• Ability to form strong alliances with marketing teams and among own team members
(c) Academic / Professional qualification / 学 历 / 专 业 资 格
Bachelor or higher degree in Science, Medical or Pharmaceutical Background
(d) Technical / skill training / 技 术 / 技 能 训 练
• Data Management Experience
• Knowledge of GCP, AZ SOPs and drug development and regulations
• Comprehensive knowledge of CDASH/SDTM/ADaM CDISC standards and metadata management
Skills for CRF/eCRF design
• Cross-function experience in drug development, particularly CRF/eCRF design and DM
• Ability to see cross-project dependencies and act to resolve issues
• Good presentation and communication skills across different business areas ( Internal , External)
• Effective meeting and time management
• Negotiation skills

(e) Working experience (No. of years / 年 资, Job function / 工 作 功 能, Business types / 业 务 种 类 )
I) Essential 必 需
• At least 5 relevant working experience in drug development or medical affair in a pharmaceutical company or CRO setting.
• Disease Area expertise in one or more therapy areas
II) Desirable 理 想
• Knowledge of observational studies and/or real world data
- III) Language ability / 语 言 能 力
• Excellent written and verbal communication skills in English and Chinese
- IV) Computer literacy / 电 脑 知 识
• PC/Windows application
- V) Others / 其 他

About this role

Summary

Manage clinical data with expertise in CDISC standards, supporting drug development projects.

Job title

Data Manager

Experience level

5+ years

Minimum experience

5+ years exp

Industry

pharmaceuticals

Location requirements

Shanghai, China; remote work not specified

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

data managementGCPCDISC standardsCRF designcommunication

Preferred skills

observational studiesreal world databilingual English Chinese

Specializations

clinical dataGCPCDISC standardsCRF/eCRF design
Locations

Structured locations inferred from the posting.

Unknown location

On-site