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Remote | Clinical Biostatistician; SDTM, ADaM & TLF
Remote / Online - Candidates ideally in
New York City, Richmond County, New York, USA
Listed on 2026-08-25
New York City, Richmond County, New York, USA
Listing for:
24-MAG LLC
Part Time, Remote/Work from Home
position Listed on 2026-08-25
Job specializations:
-
IT/Tech
Data Engineering, Data Analyst, Data Scientist
Job Description & How to Apply Below
Specialised Part-Time Consulting Opportunity for Clinical Biostatisticians
We are sharing a specialised part-time consulting opportunity for experienced clinical biostatisticians with strong expertise in Phase I–III clinical trials, SDTM and ADaM datasets, TLF production, and end-to-end statistical analysis workflows.
This role supports advanced clinical research workflows involving realistic patient-level data generation and transformation from raw clinical data through SDTM and ADaM to final tables, listings, and figures. Selected experts will ensure that statistical outputs remain internally consistent, traceable to source data, and aligned with an existing Statistical Analysis Plan.
Key Responsibilities- Generate realistic synthetic patient-level clinical trial data
- Develop data reflecting plausible patient populations, treatment patterns, outcomes, and study events
- Ensure generated datasets are clinically and statistically credible
- Maintain consistency across raw data, derived variables, analyses, and final reporting outputs
- Identify unrealistic or internally inconsistent data patterns
- Transform source clinical data into SDTM-compliant datasets
- Apply appropriate domain structures, variables, controlled terminology, and conventions
- Review datasets for completeness, consistency, and traceability
- Identify mapping or transformation issues that could affect downstream analyses
- Ensure patient-level information remains accurately represented across domains
- Develop ADaM datasets from SDTM and supporting source data
- Apply analysis derivations based on an existing Statistical Analysis Plan
- Ensure analysis populations, endpoints, baseline definitions, and derived variables are implemented correctly
- Maintain traceability between SDTM data, analysis datasets, and reporting outputs
- Review derivations for statistical and programming consistency
- Produce and validate TLF outputs for clinical trial analyses
- Ensure tables, listings, and figures reconcile to their underlying ADaM and source datasets
- Review denominators, patient counts, summary statistics, and treatment-group outputs
- Identify inconsistencies between patient-level records and aggregate results
- Ensure every reported figure can be traced back through the analysis pipeline
- Translate an existing Statistical Analysis Plan (SAP) into executable data transformations and analyses
- Implement planned endpoints, analysis populations, statistical methods, and reporting conventions
- Execute end-to-end analysis workflows across clinical trial datasets
- Validate results for statistical accuracy and internal consistency
- Apply experienced biostatistical judgement when interpreting ambiguous or complex specifications
- Verify consistency across raw data, SDTM, ADaM, and TLF layers
- Confirm that patient-level events and measurements propagate correctly into final outputs
- Identify discrepancies introduced during transformation or derivation
- Review data lineage and traceability across the full analysis pipeline
- Ensure final outputs remain reconcilable to their underlying source data
- Design realistic biostatistics and clinical-data analysis assignments
- Develop clear task instructions and expected deliverables
- Produce authoritative reference outputs for statistical workflows
- Define objective criteria for accuracy, traceability, statistical validity, and completeness
- Create tasks that reflect authentic Phase I–III biostatistics practice
- 5+ years of professional biostatistics experience, with 10–25 years preferred
- Hands-on experience across SDTM, ADaM, and TLF workflows
- Demonstrated experience supporting pre-market Phase I–III clinical trials
- Strong ability to translate an existing SAP into data transformations, analysis datasets, and reporting outputs
- Experience producing and validating patient-level clinical data and statistical outputs
- Strong understanding of dataset traceability and reconciliation across the clinical analysis lifecycle
- Ability to generate synthetic clinical data that is realistic and internally consistent
- Master's degree in Biostatistics or Statistics required
- PhD in Biostatistics, Statistics, or a closely related field preferred
- Strong statistical judgement and attention to…
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