Biostatistician — Remote/Hybrid, CDISC & Trial Design

BioPhase; New Jersey; Hybrid; USD 110,000 - 140,000; Full time

Benefits offered by this job

Hybrid work model

On-site in Parsippany, NJ

Job summary

BioPhase is seeking an experienced Biostatistician to support clinical development and post-marketing activities within a pharmaceutical setting. The role involves collaboration with biostatistics, programming, clinical teams, CROs, and external vendors to design, analyze, and report clinical studies.

The candidate should hold a master's degree in statistics/biostatistics, have 4+ years of biostatistics experience, SAS expertise, and CDISC SDTM/ADaM proficiency.

Qualifications

• Master's degree in Statistics, Biostatistics, or related field.
• 4+ years of biostatistics experience in biotech/pharma.
• Experience with randomized controlled trials.
• Strong knowledge of trial design, including adaptive designs.
• Extensive hands-on CDISC, SDTM and ADaM experience.
• Strong SAS programming experience.
• Knowledge of regulatory requirements and guidelines.
• Strong communication and cross-functional collaboration skills.

Responsibilities

• Support biostatistical activities across development and post-marketing programs.
• Contribute to the design, analysis, and reporting of randomized controlled clinical trials.
• Develop and review statistical deliverables and analyses.
• Partner with statistical programmers, clinical teams, CROs, and vendors.
• Support CDISC-compliant data standards, including SDTM and ADaM.
• Apply statistical methodologies to support clinical and regulatory decision-making.
• Communicate statistical concepts and results to technical and non-technical stakeholders.
• Manage multiple projects and timelines while maintaining high-quality deliverables.

Skills

SAS programming

Randomized trials

Biostatistics experience

Trial design knowledge

Cross-functional collaboration

Education

Master's degree in Statistics/Biostatistics

Tools

CDISC SDTM/ADaM

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Job description

BioPhase is seeking an experienced Biostatistician to support clinical development and post-marketing activities within a pharmaceutical setting. The role involves collaboration with biostatistics, programming, clinical teams, CROs, and external vendors to design, analyze, and report clinical studies.

The candidate should hold a master's degree in statistics/biostatistics, have 4+ years of biostatistics experience, SAS expertise, and CDISC SDTM/ADaM proficiency.