Remote Biostatistician for Clinical Trials & Submissions

Hire Feed

Pistoia

Remoto

EUR 78.000 - 113.000

Tempo pieno

6 giorni fa
Candidati tra i primi
Generatore di candidature

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Descrizione del lavoro

Hire Feed is hiring a Biostatistician to work remotely on a full-time basis, analyzing clinical trial data and designing statistical methodologies for regulatory submissions.

The role requires SAS/R/Python proficiency, experience with clinical trials and FDA/EMA guidelines, and the ability to communicate complex results to non-statistical stakeholders. This is a remote, global opportunity with cross-functional collaboration.

Competenze

  • Proficiency in SAS, R or Python for data analysis and visualization.
  • Experience designing statistical methodologies for clinical trials and regulatory submissions.
  • Strong biostatistical foundations including survival analysis, regression, and longitudinal data.
  • Ability to interpret and communicate complex statistical findings to non-statistical stakeholders.
  • Knowledge of FDA/EMA or other regulatory guidelines for clinical trial data analysis.

Mansioni

  • Design and implement statistical plans for clinical trials, including sample size calculations and power analyses.
  • Perform statistical analysis of clinical trial data using SAS, R, or Python to support regulatory submissions.
  • Develop statistical models to evaluate safety and efficacy endpoints in clinical trials.
  • Collaborate with cross-functional teams including clinicians, data managers, and regulatory affairs to ensure alignment with study objectives.
  • Prepare statistical sections of clinical study reports, including tables, figures, and listings.

Conoscenze

SAS
R
Python
Regulatory submissions
Survival analysis

Descrizione del lavoro

Hire Feed is hiring a Biostatistician to work remotely on a full-time basis, analyzing clinical trial data and designing statistical methodologies for regulatory submissions.

The role requires SAS/R/Python proficiency, experience with clinical trials and FDA/EMA guidelines, and the ability to communicate complex results to non-statistical stakeholders. This is a remote, global opportunity with cross-functional collaboration.

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