Biostatistics Lead, Clinical Trials & SAS/R Expert

Pacira BioSciences, Inc.; Littleton (NJ); On-site; USD 120,000 - 165,000; Full time

Benefits offered by this job

Medical, Dental & Vision

401(k) with company match

Paid holidays

Flexible time off (FTO)

Life insurance

Disability coverage

Mental Health Resources

Job summary

Pacira BioSciences, Inc. in New Jersey seeks a Senior Manager, Biostats to lead design and execution of clinical studies, engage CROs, and oversee protocol development, SAPs, and study-level BIOMETRICS discussions.

The role requires expert SAS or R programming, extensive knowledge of statistical methods, and collaboration with clinical, regulatory, data management, and external vendors to ensure high-quality results.

Qualifications

• Master's degree or PhD in Statistics or related field with clinical trial experience.
• Minimum 5 years programming in SAS/SQL with pharma industry experience.
• Minimum 3 years’ experience managing projects.

Responsibilities

• Develop statistical analysis plans for data and outputs.
• Create SAS programs or validate data/outputs.
• Provide QC on analytical outputs and ensure best practices.
• Guide programmers (Pacira and vendors) to ensure accuracy.

Skills

SAS programming

R programming

SQL

Project management

Vendor management

Biostatistics

Data validation

Statistical analysis

Written English

Education

MS in Statistics/related field

PhD in Statistics

Tools

SAS

R

SQL

Job description

Pacira BioSciences, Inc. in New Jersey seeks a Senior Manager, Biostats to lead design and execution of clinical studies, engage CROs, and oversee protocol development, SAPs, and study-level BIOMETRICS discussions.

The role requires expert SAS or R programming, extensive knowledge of statistical methods, and collaboration with clinical, regulatory, data management, and external vendors to ensure high-quality results.