Remote Colombia: Senior Statistical Programmer (SAS/SDTM)

MMS Holdings Inc; Bogotá ciudad; Hybrid; COP 60,000,000 - 90,000,000; Full time

Job summary

MMS Holdings Inc. is seeking a senior Statistical Programmer to join our data-focused clinical research team.

This full-time role is remote within Colombia and requires expertise in SAS programming, CDISC SDTM/ADaM, and generating tables, listings, and graphs from trial data. Ideal candidates have a Master's degree, 5+ years of statistical programming experience in pharma/ CRO environments, strong problem-solving skills, and familiarity with 21 CFR Part 11, FDA, and GCP guidelines.

Qualifications

• Masters required for all Statistics roles.
• Minimum of 5 years' experience in Statistical Programming or similar field required.
• Expert knowledge of scientific principles and concepts.
• Reputation as emerging leader in field with sustained performance and accomplishment.
• Proficiency with MS Office applications.
• Hands-on experience with clinical trial and pharmaceutical development preferred.
• Good communication skills and willingness to work with others to clearly understand needs and solve problems.
• Excellent problem-solving skills.
• Good organizational and communication skills.
• Familiarity with current ISO 9001 and ISO 27001 standards preferred.
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
• Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

Responsibilities

• Lead study or small programming project teams.

Skills

SAS programming

SAS Base

SAS Macros

SDTM

ADaM

E-Submission standards

Regulatory knowledge

Data pooling

MS Office

Leadership

Education

Master's degree in Statistics/Biostatistics

Tools

MS Office

Job description

MMS Holdings Inc. is seeking a senior Statistical Programmer to join our data-focused clinical research team.

This full-time role is remote within Colombia and requires expertise in SAS programming, CDISC SDTM/ADaM, and generating tables, listings, and graphs from trial data. Ideal candidates have a Master's degree, 5+ years of statistical programming experience in pharma/ CRO environments, strong problem-solving skills, and familiarity with 21 CFR Part 11, FDA, and GCP guidelines.