Data Management Consultant – Statistical Computing Environment

Eliassen Group is seeking a part-time Data Management Consultant for a fully remote role focused on implementing a Statistical Computing Environment for biometrics and clinical development. Responsibilities include defining data standards, supporting data flow design, and advising on validation and regulatory readiness. Candidates should have 8+ years of experience in Clinical Data Management and a strong understanding of CDISC standards.
Data Management Consultant – Statistical Computing EnvironmentAnywhereType: ContractCategory: Biometric & Bio PharmaIndustry: Life SciencesWorkplace Type: RemoteReference -Date Posted: 04/13/2026Rate: $100.00 to $90.00/hr. w2RemoteOur 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.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.Experience Requirements: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.Equal Opportunity Employment StatementEliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affɪrmative Mission Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.#J-18808-Ljbffr