Senior Statistical Programmer - South Africa Remote
Senior Statistical Programmer - South Africa Remote
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1 Vacancy
Job Description
Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is a awardwinning datafocused 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 industryleading 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 follow MMS on LinkedIn.
Senior Statistical Programmer
Job Specific Skills:
- Mastery and trained ongenerating 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 ESubmission 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 knowledge of ICH 21CRF Part 11 and ISO 9001:2000 requirements.
- Advanced experience with pooling of data sets for submissions.
- Advanced experience with BIMO outputs Reviewers Guides SDSP.
- Lead study or small programming project teams.
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.
- Handson 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 problemsolving 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.
Should you not have received a response within 14 days of your application please consider your application unsuccessful.
Required Experience:
Senior IC
Employment Type
Full-Time
