Biostatistics Lead — Clinical Development

Pacira BioSciences, Inc.; Littleton (NJ); On-site; USD 102,000 - 140,000; Full time

Benefits offered by this job

Medical coverage

401(k) with company match

Paid holidays

Flexible Spending Account

Job summary

Pacira BioSciences, Inc. is seeking a Manager, Biostatistics to lead statistical activities across clinical development programs and post-marketing efforts.

The role collaborates with biostatisticians, programmers, CRO partners, and cross-functional teams to deliver high-quality analyses for regulatory decisions. The successful candidate will support development and review of statistical deliverables, contribute to study design, and engage with regulatory authorities on statistical topics,

Qualifications

• Master’s Degree in statistics/biostatistics from an accredited institution.
• Minimum 2 years in biotech/pharmaceuticals industry.
• Experience in statistical design, analysis and reporting of randomized controlled trials.

Responsibilities

• Provide statistical leadership for one or more clinical development programs, ensuring consistency and quality of deliverables.
• Manage statistical responsibilities of clinical studies from program development through CSR creation and publication, collaborating with statisticians and programmers.
• Serve as the primary statistical point of contact for assigned programs and studies.
• Support protocol development and study design.

Skills

Statistical leadership

Clinical trial design

Statistical analysis

SAS programming

CDISC standards

Regulatory interactions

Cross-functional collaboration

R programming

Education

Master’s Degree in statistics/biostatistics

Tools

SAS

R

Job description

Pacira BioSciences, Inc. is seeking a Manager, Biostatistics to lead statistical activities across clinical development programs and post-marketing efforts.

The role collaborates with biostatisticians, programmers, CRO partners, and cross-functional teams to deliver high-quality analyses for regulatory decisions. The successful candidate will support development and review of statistical deliverables, contribute to study design, and engage with regulatory authorities on statistical topics,