Biostatistician

Placements24; Riverton (UT); Remoto; USD 90.000 - 150.000; Tempo pieno

Vantaggi offerti da questo lavoro

Comprehensive health insurance

Remote work environment

Professional development opportunities

Descrizione del lavoro

Placements24 is seeking a highly analytical Biostatistician for a fully remote role within a dynamic research team. You will design analysis plans, perform complex modeling in SAS/R, interpret results for regulatory submissions, and collaborate with scientists and data managers to ensure data quality.

The ideal candidate has a Master’s or PhD in Statistics/Biostatistics, at least 4 years in pharma/biotech, and strong communication skills.

Competenze

• Master’s or PhD in Statistics or Biostatistics or related field.
• Minimum 4 years of Biostatistics experience in pharma/biotech.
• Proficiency in SAS or R.
• Strong understanding of clinical trial design and regulatory requirements.
• Experience with survival and longitudinal analyses.

Mansioni

• Design statistical analysis plans for clinical trials and observational studies.
• Perform statistical analyses of clinical trial data using SAS/R/SPSS.
• Interpret results and prepare reports for internal stakeholders and regulatory agencies.
• Collaborate with clinical operations and data management to ensure data quality.
• Contribute to study protocols and statistical sections of documents.
• Stay updated with advancements in statistical methods for pharmaceutical research.

Conoscenze

Statistical analysis

SAS/R programming

Communication

Formazione

Master's or PhD in Statistics/Biostatistics

Strumenti

SAS

R

SPSS

Descrizione del lavoro

About the Role

Our client is seeking a highly analytical and proficient Biostatistician to join their dynamic research team, operating in a fully remote capacity. This role is crucial for the design, analysis, and interpretation of clinical trial data, ensuring the integrity and validity of scientific findings. You will work closely with clinical scientists, data managers, and other researchers to develop statistical analysis plans, perform complex statistical modeling, and contribute to regulatory submissions. This is an exceptional opportunity for a skilled statistician to contribute to groundbreaking pharmaceutical research from a remote location.

Key Responsibilities

• Design statistical analysis plans for clinical trials and observational studies.
• Perform statistical analysis of clinical trial data using appropriate software (e.g., SAS, R, SPSS).
• Interpret statistical results and prepare reports for internal stakeholders, regulatory agencies, and publications.
• Collaborate with clinical operations and data management teams to ensure data quality and integrity.
• Contribute to the development of study protocols, statistical sections of investigator brochures, and other study documents.
• Stay current with advancements in statistical methodologies and their application in pharmaceutical research.

Requirements

• Master's or Ph.D. in Statistics, Biostatistics, or a related quantitative field.
• Minimum of 4 years of experience as a Biostatistician in the pharmaceutical or biotechnology industry.
• Proficiency in statistical programming languages such as SAS or R.
• Strong understanding of clinical trial design, statistical principles, and regulatory requirements for drug development.
• Experience with survival analysis, longitudinal data analysis, and other advanced statistical techniques.
• Excellent problem-solving abilities and strong written and verbal communication skills.

Benefits

• Competitive annual salary and performance-based incentives.
• Comprehensive health, dental, and vision insurance coverage.
• Flexible remote work environment, promoting work-life balance.
• Generous professional development opportunities, including access to training and conferences.
• The chance to work on innovative projects that impact global health.