Senior Manager, Biostatistics

Jobtailor; Madison (NJ); On-site; USD 120,000 - 160,000; Full time

Job summary

Jobtailor is seeking an experienced Biostatistician/Statistician to design and analyze clinical studies, interpret results, and prepare study reports under supervision. You will translate scientific questions into statistical terms and collaborate with cross-functional teams to ensure high-quality deliverables.

Requirements include a PhD with 3+ years or an MS with 5+ years in statistics/biostatistics, proficiency in SAS/R/Python, and strong communication and writing skills.

Qualifications

• Fresh PhD with 3+ years or MS with 5+ years in statistics/biostatistics with clinical trials or healthcare experience.
• Proficiency in SAS, R or Python and implementation of advanced statistical analysis, data manipulation, graphing or simulation.
• Good interpersonal, communication, writing and organizational skills.
• Ability to learn regulatory requirements, clinical trial design, data analysis and interpretation, and work in cross-functional teams.
• Experience with standard and advanced statistical methods; understanding regulatory requirements and trial design is preferred.

Responsibilities

• Collaborates in design of clinical study including methodology, data analysis and interpretation, and reporting of study results.
• Authors/reviews protocol synopsis, protocols, SAPs, CRFs, clinical study reports and other study documents with minimal supervision.
• Performs/validates statistical analyses and advises on clarity of data display.
• Communicates results to cross-functional teams and contributes to study documents and publications.
• Translates scientific questions into statistical terms and presents concepts in layman terms.
• Ensures compliance with processes/SOPs and maintains quality of deliverables.

Skills

Statistical analysis

Clinical trial design

Data interpretation

Interpersonal skills

Communication skills

Writing skills

Education

PhD

MS

Tools

SAS

R

Python

Job description

• Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results.
• Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents with minimum supervision
• Performs and/or validates statistical analyses, advise ways to maximize clarity of data display
• Communicates results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications.
• Translates scientific questions into statistical terms and statistical concepts into layman terms.
• Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable.
• Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results.
• Continually enhances knowledge of drug development process, regulatory and commercial requirement
• Develops & advises team members. Effectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS.

Requirements

• Fresh PhD with 3+ years’ experience or MS with 5+ years’ experience in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience
• Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation.
• Good interpersonal, communication, writing and organizational skills
• Ability to: learn regulatory requirements & clinical trial design, data analysis and interpretation, work successfully within cross-functional teams, organize multiple work assignments and establish priorities
• Experience in standard and advanced statistical methods is preferred.
• Good understanding of regulatory requirements & clinical trial design is preferred.

Core Competencies

Demonstrates expertise in statistical analysis and clinical trial design, with proficiency in SAS, R, or Python for data manipulation and advanced statistical methods. Strong communication skills facilitate effective collaboration and interpretation of complex data for cross-functional teams.

Highest-signal resume keywords

• Statistical Analysis
• Clinical Trial Design
• SAS Programming
• R Programming
• Data Interpretation

ATS Optimization Keywords

Hard Skills

• Biostatistics
• Data Manipulation
• Graphing
• Simulation
• Statistical Methods

Soft Skills

• Interpersonal Skills
• Communication Skills
• Organizational Skills
• Writing Skills

Industry Keywords

• Clinical Trials
• Drug Development
• Pharmaceutical Industry
• Regulatory Requirements
• Healthcare

Tools & Technologies

• SAS
• R
• Python