Biostatistician (Remote)

Role: Biostatistician (Remote) Location: Remote (Work from Anywhere) Job Type: Contract Payout: $60 - $65/hour Role Overview: We are hiring for one of our clients, seeking a Biostatistician to work on a contract basis. The role involves analyzing clinical trial data and ensuring compliance with regulatory standards. Primary tasks include designing statistical methodologies, conducting data analysis, and preparing reports for submission to health authorities. Key Responsibilities: • 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. Required Skills & Qualifications: • Proficiency in statistical software such as SAS, R, or Python for data analysis and visualization. • Experience in designing statistical methodologies for clinical trials and regulatory submissions. • Strong understanding of biostatistical principles, including survival analysis, regression modeling, and longitudinal data analysis. • 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. More About the Opportunity: This role offers a unique opportunity to work with a global leader in the pharmaceutical manufacturing industry, contributing to the development of life-saving therapies. The position involves high-impact projects with direct influence on regulatory approvals. Equal Opportunity Employer: We hire based on skills and expertise. All qualified candidates are welcome regardless of background, experience, or prior employment history. Applications are reviewed solely on demonstrated technical ability and qualifications. Apply Now!

The Biostatistician will design statistical plans and implement methodologies for clinical trials to support regulatory submissions. They will analyze safety and efficacy endpoints and prepare statistical sections of clinical study reports.

Candidates must be proficient in SAS, R, or Python and have experience with clinical trial design and regulatory guidelines. Strong knowledge of biostatistical principles like survival analysis and regression modeling is required.

• Visualisation de donnéesSouhaitée
• PythonSouhaitée

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

• SAS
• R
• Python
• Clinical Trial Design
• Statistical Analysis
• Regulatory Submissions
• Sample Size Calculation
• Power Analysis
• Survival Analysis
• Regression Modeling
• Longitudinal Data Analysis
• Data Visualization
• FDA Guidelines
• EMA Guidelines
• Clinical Study Reports

• Science & Research
• Healthcare
• Data & Analytics
• Manufacturing

Expérience minimale

2+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Associate