Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being
Summary of Responsibilities: Perform the role of the Lead Statistical Programmer. Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction
Description The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of
Overview Habilidades, experiencia, cualificaciones. Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo. In this role you will design, build, and optimize interactive R Shiny applications that support clinical trial activities, enabling
En ALTEN sabemos que el éxito de nuestros proyectos se debe a las personas que forman parte de nuestro equipo. Por eso, si tienes experiencia en Statistical Programming con SAS y quieres participar en proyectos internacionales
En ALTEN sabemos que el éxito de nuestros proyectos se debe a las personas que forman parte de nuestro equipo. Por eso, si tienes experiencia en Statistical Programming con SAS y quieres participar en proyectos internacionales
We’re expanding across Mexico, Brazil, Argentina, Colombia, Chile, and Peru , and we’re looking for a Senior Clinical Database Programmer to help build the foundation of our clinical data operations in LATAM. In this high-impact role,
Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team?MMS is aaward-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great
MMS Holdings Inc is a data-focused clinical research organization (CRO) seeking a Senior Statistical Programmer. The role requires a Masters and at least 5 years of experience in Statistical Programming, with expertise in SAS, SDTM/ADaM and regulatory
The Senior Clinical Data Manager will lead and manage multiple clinical studies, ensuring that data are collected, managed and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in
The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard
Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being