MMS Holdings Inc in South Africa is looking for a Statistical Programmer II. This role requires a Masters degree in Statistics along with a minimum of 3 years of experience in statistical programming. The ideal candidate must
Parexel International is looking for a Statistical Programming Lead in South Africa. This role requires a dedicated expert to provide technical support during clinical trials and oversee programming activities while ensuring strict adherence to quality standards. The ideal
IQVIA is seeking a Principal Statistical Programmer to work homebased in South Africa. This role involves reviewing datasets, ensuring submission readiness, and leading SAS programming efforts for clinical trials. The ideal candidate will have a BSc in a
Borbet SA in Gqeberha is seeking a Software Developer to assist with system integration tasks and project oversight. Responsibilities include SCADA monitoring, compliance regulation updates, and programming tasks in languages such as C++ and Python. The ideal candidate
This position is available in the following EMEA locations – South Africa, Lithuania, Poland and we offer fully remote home-based working. Picture Yourself At Parexel: The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and
About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four
ABOUT US Data EQ uses social media and other customer feedback data to help our clients (large enterprise brands) generate better CX insights, manage risk, improve conduct reporting and optimise social customer service. Data is at
Location: Homebased in South Africa, no travel / fully remote Business Unit: Clinical FSP, sponsor-dedicated The Principal Statistical Programmer will be responsible for the review of datasets in submission ready standard format (ADa M), tables, figures,
Your responsibilities Project Management for our biostatistical services, provide technical supervision and lead project teams in all biostatistical activities of clinical trials. You act as the primary point of contact for our project clients. You manage