Clinical Data Configuration Specialist: Rave/Veeva : Max 12 LPA :Apply
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Clinical Data Configuration Specialist: Rave/Veeva : Max 12 LPA :Apply

Date Posted
14 July 2026
Location
Hyderabad
Positions
1
Views
5
Employment Information
Open Positions
1
Location
Hyderabad
Address
Hyderabad, Bengaluru, Mumbai (All Areas)
Experience
5 Years
Functional Area
Design
Job Description

Role: Healthcare & Life Sciences - Other

Industry Type: BPM / BPO

Department: Healthcare & Life Sciences

Employment Type: Full Time, Permanent

Role Category: Healthcare & Life Sciences - Other

UG: Any Graduate

Hi, We are hiring for one of India's leading IT & consulting organizations for the position of Clinical Data Configuration Specialist Role. Summary A Clinical Data Configuration Specialist is a technical professional who manages, structures, and validates data collected during clinical trials. They specialize in configuring Electronic Data Capture (EDC) systems, setting up study databases, and ensuring data formats meet regulatory standards using tools like SQL, SAS, or Python. To Apply for above Clinical Data Configuration Specialist, WhatsApp 'Hi' @ 9519459922 When Asked For The job Code, Type: Job Code # 5

Key Skills

Minimum 4 years of experience with EDC build or data extraction configuration ETL/ELT experience Understanding of AWS/Data bricks concepts Experience developing R shiny and Python apps Any Graduate

Key Responsibilities

Configure data extraction and transformations in an individual contributor role across multiple data sources at the study level as defined by the Data Transfer Agreement and other specifications provided by Data Engineer Partner closely with internal/external stakeholders and data engineers in a collaborative manner Ensure accurate delivery of data format and data frequency with quality deliverables per specification Assist with quality review of activities performed by a vendor, as needed Experience with EDC build, Data Management, and EDC extraction configuration Knowledge of data flow between clinical data management systems, vendor devices, and CDR Knowledge of XMLS, ALS, APIs, and MDR preferred Experience with one of these languages: SQL, SAS, R, Python Understanding of SDTM Strong working knowledge of clinical trial terminology and data transfer specifications Demonstrated ability to lead projects and work groups with strong project management skills Proven ability to resolve problems independently and collaboratively Ability to work in a fast-paced environment with demonstrated ability to juggle and prioritize multiple competing tasks and demands Ability to work independently, take initiative, and complete tasks within deadlines Strong attention to detail and organizational skills Good time management skills Quick learner with the ability to ask questions and adapt to new technologies and systems Good knowledge of office software (Microsoft Office)

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