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, you’ll lead the development,
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, you’ll lead the development,
The eClinical / Medidata Database Programmer is responsible for building, configuring, testing, and maintaining clinical study databases and related eClinical system components. This role supports clinical trial study startup, database build, edit check programming, system configuration, user acceptance testing,
When our values align, theres no limit to what we can achieve. Parexel FSP is hiring for multiple Clinical Data Manager positions in Colombia, Mexico, Argentina, and/or Brazil. Job Purpose: The Clinical Data Manager will be responsible for
The Statistical Programmer will be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM)
Study Lead Programmer - Argentina ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to
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 Data Tabulation
Job Overview Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In
jobr.pro is seeking a Principal Biostatistician to lead design, analysis, and interpretation of clinical studies within a collaborative team. The role involves oversight of statistical output, study protocols, and safety reviews, working with sponsor teams, PMs, data
Job Description The Principal Biostatistician is responsible for the design, analysis, and/or interpretation of clinical studies as a lead (or contributing team member) for clinical studies. In this role, the Principal Biostatistician will be part of a collaborative