Biostatistician

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

R

Job description

• Remote/Hybrid - hybrid in Parsippany, NJ
• Contract end date: 3/19/27

We are seeking an experienced Biostatistician to support clinical development and post-marketing activities within a pharmaceutical environment. This individual will collaborate with biostatistics, statistical programming, clinical teams, CROs, and external vendors to support the design, analysis, and reporting of clinical studies.

Responsibilities

• Support biostatistical activities across clinical 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

Qualifications

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

Preferred

• Experience with R
• Regulatory submission/interaction experience
• Knowledge of real-world evidence, observational research, or causal inference
• Experience supporting acute or chronic pain clinical programs