Senior Statistical Programmer: Lead Clinical Data & SAS

MMS Holdings Inc; Northern (KY); Hybrid; USD 90,000 - 140,000; Full time

Job summary

MMS Holdings Inc is seeking a Senior Statistical Programmer to lead programming efforts for clinical trial data. You will generate tables, listings, and graphs from study databases using SAS, and apply SDTM/ADaM standards in submissions.

The role requires Masters in statistics or related field, 5+ years of experience in statistical programming, and strong knowledge of regulatory guidelines (FDA, GCP). Collaborative, detail-oriented professionals will thrive in MMS's team-focused environment.

Qualifications

• Masters required for Statistics roles.
• Minimum 5 years in Statistical Programming or similar field.
• Expert knowledge of scientific principles.
• Reputation as emerging leader with sustained performance.
• Familiarity with ISO 9001 and ISO 27001 preferred.
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements.

Responsibilities

• Lead study or small programming project teams.
• Generate tables, listings, and graphs from trial data using SAS.

Skills

SAS programming

TFL generation

SDLC experience

SAS Macros

ADaM/SDTM knowledge

Data pooling for submissions

Lead programming projects

Communication skills

Regulatory knowledge

Education

Masters required for Statistics roles

Tools

SAS Base

SAS Macros

MS Office

Job description

MMS Holdings Inc is seeking a Senior Statistical Programmer to lead programming efforts for clinical trial data. You will generate tables, listings, and graphs from study databases using SAS, and apply SDTM/ADaM standards in submissions.

The role requires Masters in statistics or related field, 5+ years of experience in statistical programming, and strong knowledge of regulatory guidelines (FDA, GCP). Collaborative, detail-oriented professionals will thrive in MMS's team-focused environment.