Lead SAS Programmer for Phase 3 Clinical Trials

Integrated Resources Inc.; Woodcliff Lake (NJ); On-site; USD 80,000 - 120,000; Full time

Job summary

A leading clinical research organization is seeking a skilled professional to support phase 3 clinical trials. The ideal candidate will have a Master's degree in Biostatistics and extensive experience in SAS programming and clinical data standards. This role involves ensuring high-quality data through proactive monitoring, statistical analysis, and effective communication with regulatory bodies. Join a dynamic team dedicated to delivering impactful healthcare solutions.

Qualifications

• Preferred MS in Biostatistics/Statistics with 5 years experience.
• Strong skills in SAS, CDISC standards, and technical writing.
• Experience in a high-pressure environment managing multiple projects.

Responsibilities

• Supports phase 3 clinical trials, develops quality surveillance plans.
• Validates statistical analysis and interprets clinical study reports.
• Liaises with statisticians and supports regulatory communication.

Skills

SAS programming

CDISC data standards

Technical writing

Communication

Organizational skills

Teamwork ability

Education

MS in Biostatistics/Statistics

Tools

UNIX

Windows

Job description

A leading clinical research organization is seeking a skilled professional to support phase 3 clinical trials. The ideal candidate will have a Master's degree in Biostatistics and extensive experience in SAS programming and clinical data standards. This role involves ensuring high-quality data through proactive monitoring, statistical analysis, and effective communication with regulatory bodies. Join a dynamic team dedicated to delivering impactful healthcare solutions.