- 经验
- 5年以上
- 薪水
- —
- 职位空缺
- 1
- 发布
- 1 小时前
- 工作模式
- 在办公室
- 合格
- Professionals with a minimum of 5 years of EDC database build experience in clinical research, including experience in clinical trials, Medidata Rave, and global cross-functional environments. UK visa sponsorship is not available.
- 恢复
- 需要申请
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职位描述
Role overview
The EDC Data Acquisition Expert is responsible for defining, building, and putting into practice clinical electronic data capture tools and the related documents and workflows that support protocol-driven data collection in clinical trials. This position works closely with data managers, study responsible physicians, study responsible scientists, and biostatisticians.
Key responsibilities
- Review protocol-level data capture needs and assemble the study start-up eCRF package using global eCRF libraries.
- Create the eCRF structure and layout, including dynamic form behavior.
- Develop edit checks and custom functions.
- Prepare technical specifications for tSDV, Safety Gateway integration, and Datamart mapping.
- Set up EDC coding configurations in line with study-specific coding rules.
- Carry out testing and production migration for Rave EDC.
- Coordinate the planning, requirements, and delivery of IWRS integrations with EDC.
- Act as a technical expert for complex EDC database builds, including integrations.
- Act as a technical expert for advanced custom function implementation within database builds.
- Train junior team members on EDC build, migration processes, and supporting tools.
- Contribute to ongoing process, system, and tool enhancement efforts within clinical data management.
Experience and technical requirements
- At least 5 years of experience creating EDC databases for clinical research.
- Hands-on experience building complex Medidata Rave EDC databases.
- Strong project management capability.
- Advanced knowledge of custom function programming.
- Background working on clinical trials.
- Experience in diverse, cross-functional, global, and multi-regional clinical research teams.
- Working understanding of GCP and ICH guidelines.
- Knowledge of CDASH.
Additional information
This position is not eligible for UK visa sponsorship.
About the employer
IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare sectors, supporting the development and commercialization of innovative treatments to improve patient outcomes and population health.
Hiring integrity
The company maintains a zero-tolerance approach to candidate fraud. All details and credentials provided during recruitment must be accurate and complete. Any false information, misrepresentation, or material omission may lead to immediate disqualification or later termination of employment, subject to applicable law.