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: Reviews study protocol and assists study team in the implementation of routine clinical data management process
including data entry, data quality checking to meet the protocol requirements in a timely manner
Assists in the preparation of Case Report Form and Study Worksheet for data collection
Manage and tracks routine data entry
Manage, identifies, tracks and resolves routine queries
Utilizes/Develop routine reports to track study progress and ensures timeliness and quality expectations are met
Demonstrates understanding of project timelines and metrics to ensure data are delivered to timelines
Supports and participates in the continuous improvement of quality data and data management process
Adheres to HIPAA and 21CFR Part 11 requirements
Help to establish standard processes and procedures for Data Management department
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: attractive salary
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- Masters or Bachelors degree in Medical informatics/MIS/nursing/pharmacy/healthcare/ or at least 1 year of relevant experience
- Clinical background or experience in a healthcare field, pharmaceutical vendor or information technology firm preferred
- Experience related to research with knowledge of research principles, methodologies and study design. CITI certification preferred
- Good English written and communication skills
- Good working knowledge of MS Word, MS Excel and MS Access
- Deadline oriented
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- HIV-NAT HIV-NAT
: - Email
[Confidential Information]
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