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Data Acquisition Expert (eSource Specialist)(m/w/x)
Description
You will bridge the gap between clinical data and technology by automating data entry through EHR and EDC integration, ensuring seamless data flow and study readiness across clinical trials.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •5 years' experience in clinical data management
- •Experience in EHR/EMR and EDC integration
- •Knowledge of EDC and study design
- •Understanding of clinical trial standards
- •Excellent problem-solving and adaptability
- •Knowledge of clinical research methodologies
- •Outstanding written and verbal communication
- •Ability to work collaboratively
- •Ineligibility for UK visa sponsorship
Work Experience
5 years
Tasks
- •Acquire and analyze EHR/EMR data
- •Integrate data with EDC systems
- •Ensure site and study readiness
- •Update eCRF forms with study teams
- •Assess study production and deployment status
- •Identify migration needs and relevant fields
- •Prepare detailed integration specification documents
- •Maintain expert knowledge of EDC systems
- •Apply FHIR and EHR data standards
- •Utilize clinical trial design knowledge
- •Adapt to new technologies and methodologies
- •Solve complex technical problems efficiently
- •Communicate with team members and stakeholders
- •Coordinate cross-functional integration activities
Tools & Technologies
Languages
English – Business Fluent
- EYFull-timeWith HomeofficeSeniorBerlin, Düsseldorf, Frankfurt am Main, Hamburg, Köln, Mannheim, München, Stuttgart
- IQVIA
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Data Acquisition Expert (eSource Specialist)(m/w/x)
The AI Job Search Engine
Description
You will bridge the gap between clinical data and technology by automating data entry through EHR and EDC integration, ensuring seamless data flow and study readiness across clinical trials.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •5 years' experience in clinical data management
- •Experience in EHR/EMR and EDC integration
- •Knowledge of EDC and study design
- •Understanding of clinical trial standards
- •Excellent problem-solving and adaptability
- •Knowledge of clinical research methodologies
- •Outstanding written and verbal communication
- •Ability to work collaboratively
- •Ineligibility for UK visa sponsorship
Work Experience
5 years
Tasks
- •Acquire and analyze EHR/EMR data
- •Integrate data with EDC systems
- •Ensure site and study readiness
- •Update eCRF forms with study teams
- •Assess study production and deployment status
- •Identify migration needs and relevant fields
- •Prepare detailed integration specification documents
- •Maintain expert knowledge of EDC systems
- •Apply FHIR and EHR data standards
- •Utilize clinical trial design knowledge
- •Adapt to new technologies and methodologies
- •Solve complex technical problems efficiently
- •Communicate with team members and stakeholders
- •Coordinate cross-functional integration activities
Tools & Technologies
Languages
English – Business Fluent
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
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