Clinical Biostatistician | $65/hr Remote

Position: Biostatistician Type: Contract Compensation: $60 - $65/hour Location: Remote Commitment: 10-40 hrs/week Role Responsibilities Author and review evaluation tasks for deriving, reproducing, or validating statistical outputs from clinical datasets. Assess correctness and consistency of reported estimates, confidence intervals, and p-values in alignment with SAP. Identify discrepancies between statistical outputs and narrative descriptions in clinical study reports. Establish defensible ground truth for evaluation tasks, documenting the derivation process for verification. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives. Collaborate with a multidisciplinary project team to refine evaluation tasks and criteria. Requirements Have strong relevant experience in the domain supporting clinical trials at a sponsor, CRO, or academic trials unit. Hands-on experience producing or quality controlling TFLs for regulatory submissions from CDISC SDTM/ADaM datasets. Solid understanding of statistical methods used in confirmatory trials, including survival analysis and mixed models. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field. Application Process Easy Apply on LinkedIn Check email for next steps Participate in resume evaluation & interview stage

The role involves authoring and reviewing evaluation tasks to validate statistical outputs from clinical datasets. It requires identifying discrepancies between statistical results and clinical study reports while establishing defensible ground truths.

Candidates must have an advanced degree in Biostatistics or a related field and experience supporting clinical trials at a sponsor or CRO. Proficiency in SAS or R and hands-on experience with CDISC standards for regulatory submissions are required.

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Biostatistics
• Clinical Trials
• TFL Production
• CDISC SDTM
• CDISC ADaM
• Survival Analysis
• Mixed Models
• SAS
• R
• SAP Interpretation
• Quality Control
• Statistical Validation

• Science & Research
• Healthcare
• Data & Analytics

Formation minimale

Maîtrise

Expérience minimale

2+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Associate

Mode de candidature

La candidature directe est offerte