Senior Data Analyst
United States · ಒಪ್ಪಂದ
ಅರ್ಜಿ ಸಲ್ಲಿಸುವವರಲ್ಲಿ ಮೊದಲಿಗರಾಗಿರಿ
- ಅನುಭವ
- ಯಾವುದೇ
- ಸಂಬಳ
- —
- ತೆರೆಯುವಿಕೆಗಳು
- 1
- ಪೋಸ್ಟ್ ಮಾಡಲಾಗಿದೆ
- 5 ಗಂಟೆಗಳ ಹಿಂದೆ
- Work mode
- ಕಚೇರಿಯಲ್ಲಿ
- Eligibility
- Professionals with experience in clinical trial data, clinical IT, or related data standards roles who can work onsite in the United States.
- Resume
- Required to apply
ಕೆಲಸದ ವಿವರ
Role Overview
Virtual Connect Solutions is seeking a Senior Data Analyst / SME with strong expertise in clinical data standards, especially SDTM. This position is centered on supporting clinical IT work and partnering closely with business and scientific stakeholders across Biostatistics, Statistical Programming, Clinical Operations, and Clinical Data Management.
The role calls for practical, hands-on knowledge of clinical data standards and submission datasets, with a strong emphasis on producing reliable, analysis-ready data for downstream statistical work.
Core Collaboration Areas
- Work alongside Biostatistics teams to help shape study design, prepare analysis-ready data, and support submission data strategy.
- Coordinate with Statistical Programmers to help ensure analysis datasets are built and implemented correctly.
- Partner with Clinical Data Management teams to make sure source data is aligned with SDTM requirements downstream.
- Engage with Clinical Operations so operational data capture supports analysis and submission needs.
- Serve as the link between IT/data architecture and clinical study execution teams.
Technical Expertise
The ideal candidate should bring strong depth in CDISC standards, particularly SDTM and ADaM, along with a solid understanding of how clinical data is prepared for regulatory submission.
- Strong command of SDTM, including domain structures and mapping from raw clinical data.
- Knowledge of controlled terminology and SDTM implementation guidance.
- Experience creating or reviewing submission-ready SDTM datasets.
- Understanding of ADaM dataset development for statistical analysis.
- Ability to maintain traceability from SDTM to ADaM to TLFs (Tables, Listings, Figures).
- Experience with SDTM mapping specifications and transformation logic.
- Awareness of regulatory submission expectations such as FDA and PMDA requirements.
Ideal Background
- Experience in clinical trial data environments.
- Practical exposure to SDTM and ADaM dataset creation or review.
- Ability to interpret and translate between clinical/business needs, statistical analysis requirements, and technical data structures.
- Comfort participating in detailed technical conversations with biostatisticians.
- Capability to act as a communication bridge between IT/data systems and scientific teams.
Additional Information
This is a contract role based onsite in the United States.