More jobs:
Data Management Consultant – Statistical Computing Environment
Job in
Pine Bluff, Jefferson County, Arkansas, 71601, USA
Listed on 2026-06-04
Listing for:
Eliassen Group
Part Time
position Listed on 2026-06-04
Job specializations:
-
IT/Tech
Data Security, Data Analyst
Job Description & How to Apply Below
Description
Remote
Our client is implementing a Statistical Computing Environment to support biometrics and clinical development. The consultant will embed Data Management standards, structures, and traceability into the platform and align processes across IT, Biostatistics, and Programming. The role focuses on defining data flows, metadata, and CDISC implementation while advising on validation, access, and inspection readiness. The engagement is part-time and fully remote.
Rate: $100.00 to $90.00/hr. w2
Responsibilities- Partner with IT and Biostatistics stakeholders to integrate Data Management requirements into the SCE design and implementation.
- Define and document data standards, structures, metadata, and lineage requirements to ensure traceability and regulatory readiness.
- Support design of end-to-end data flows across clinical data sources, downstream analytics, and reporting within the SCE.
- Advise on process alignment between Data Management, Biostatistics, and Programming to support efficient study execution.
- Ensure Data Management considerations are incorporated into validation, access controls, audit trails, and inspection readiness activities.
- Provide practical guidance on CDISC standards (SDTM/ADaM) and how they are operationalized within the SCE.
- Identify risks, gaps, or inefficiencies related to data handling and recommend pragmatic solutions.
- Support cross-functional communication and change management as teams transition to the new environment.
- 8+ years of experience in Clinical Data Management within biotech, pharma, or CRO environments.
- Hands‑on experience working alongside Biostatistics and Statistical Programming teams.
- Strong understanding of clinical data standards, including CDISC SDTM and ADaM, and regulated data environments.
- Knowledge of data flow architecture, metadata management, and data traceability supporting clinical analysis and submissions.
- Ability to operate independently in a consultative capacity and deliver results in a fast‑paced, small biotech environment.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×