Lead SAS Programmer — Biopharma Submissions

Syneos Health; United States; On-site; USD 81,000 - 145,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, Visn

401k match

Employee Stock Purchase Plan

Paid time off

Job summary

Syneos Health is seeking a Principal Statistical Programmer for US-based hiring. The role leads programming for compound studies, maintaining timelines and standards while mentoring junior programmers. You will review CDISC validation outputs and support submissions under supervision.

The ideal candidate has 8+ years SAS/Base/Macro/GRAPH experience in biopharma or CROs, solid data management with CDISC, and strong leadership and organizational skills.

Qualifications

• BA/BS degree required; MS in statistics or computer sciences is desired.
• Minimum 8 years of programming experience using SAS/Base/Macro/GRAPH in biopharma or CROs.
• Data management experience with CDISC standards is highly desirable.
• Strong SAS programming skills and attention to detail are essential.
• Knowledge of regulatory guidelines including electronic submission standards.
• Strong organizational, time management, communication and leadership skills.

Responsibilities

• Function as a Lead programmer for a compound or group of studies.
• Maintain the overall timeline for studies and programming standards.
• Review standard macros and datasets; allocate resources for groups of studies.
• Mentor junior programmers on Incyte systems and standards.
• Assist in study set-up and identify similar studies.
• Ensure validation reports are clean and properly documented.
• Act as programming lead for submissions under supervision of management.
• Provide expert recommendations to complex problems and mentor junior staff.

Skills

SAS programming

Leadership

Time management

Communication

Project coordination

Education

BA/BS degree (MS in statistics or computer sciences desired)

Tools

CDISC

Job description

Syneos Health is seeking a Principal Statistical Programmer for US-based hiring. The role leads programming for compound studies, maintaining timelines and standards while mentoring junior programmers. You will review CDISC validation outputs and support submissions under supervision.

The ideal candidate has 8+ years SAS/Base/Macro/GRAPH experience in biopharma or CROs, solid data management with CDISC, and strong leadership and organizational skills.