Senior Statistical Programmer - South Africa (Remote) Biometrics South Africa

Mms Holdings Inc; Cape Town; Remote; ZAR 600 000 - 750 000; Full time

Job summary

A data-focused clinical research organization is seeking a Senior Statistical Programmer in Cape Town. The role requires expertise in SAS programming and a Master's degree in Statistics, alongside a minimum of 5 years’ experience. Candidates should exhibit strong problem-solving and communication abilities, with responsibilities including generating clinical trial data outputs and leading programming teams.

Qualifications

• Minimum of 5 years' experience in Statistical Programming or a similar field required.
• Expert knowledge of scientific principles and concepts.
• Hands-on experience with clinical trial and pharmaceutical development preferred.

Responsibilities

• Generate tables, listings, and graphs from clinical trial databases using SAS.
• Utilize System Development Life Cycle (SDLC) for programming deliverables.
• Lead study or small programming project teams.

Skills

SAS programming

Statistical principles

Problem-solving skills

Communication skills

MS Office proficiency

Education

Master's degree in Statistics or related field

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?

MMS is an award-winning, data-focused clinical research organization (CRO).

We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.

With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.

Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career.

Visit or follow MMS on LinkedIn.

Senior Statistical Programmer

Job Specific Skills

• Mastery and trained in generating tables, listings, and graphs from clinical trial databases using SAS.
• Utilizes System Development Life Cycle (SDLC) for programming deliverables.
• Advanced user in SAS programming, SAS Base, and SAS Macros.
• Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
• Mastery and trained on SDTM standards including ability to write specifications.
• Advanced knowledge of ADaM standards including supporting specification writing.
• Proficient with MS Office applications.
• Advanced experience with pooling of data sets for submissions.
• Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP.
• Lead study or small programming project teams.

Advanced knowledge of ICH, 21CRF Part 11, and ISO

Job Requirements

• 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 and ISO standards preferred.
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
• understanding of CROs and scientific & clinical data / terminology, and the drug development process.

Should you not have received a response within 14 days of your application, please consider your application unsuccessful.