Senior Principal Statistical Programmer — Pharma Lead

Katalyst CRO; Paramus (NJ); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading clinical research organization in Paramus, NJ is seeking a Senior Manager in Statistics to oversee statistical activities in clinical trials. The ideal candidate will have a Ph.D. or MS in Statistics and at least 4 to 6 years of experience in the pharmaceutical sector. Responsibilities include designing study elements, reviewing statistical analysis, and interacting with cross-functional teams to ensure quality and compliance. Strong knowledge of SAS and industry standards is essential, along with excellent organizational and communication skills.

Qualifications

• Minimum of 4 years (Ph.D.) or 6 years (MS) Pharmaceutical/CRO industry experience.
• Excellent knowledge of industry standards such as ICH guidelines and CDISC data structures.
• Ability to work independently and problem-solve.

Responsibilities

• Review protocol and prepare statistical sections of studies.
• Work closely with Statistical Programmers and Clinical Data Manager.
• Participate in monitoring CRO activities and reviewing CRO deliverables.

Skills

SAS computer package

Leadership

Communication

Time management

Problem-solving

Education

Ph.D. or MS in Statistics or Biostatistics

Job description

A leading clinical research organization in Paramus, NJ is seeking a Senior Manager in Statistics to oversee statistical activities in clinical trials. The ideal candidate will have a Ph.D. or MS in Statistics and at least 4 to 6 years of experience in the pharmaceutical sector. Responsibilities include designing study elements, reviewing statistical analysis, and interacting with cross-functional teams to ensure quality and compliance. Strong knowledge of SAS and industry standards is essential, along with excellent organizational and communication skills.