Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data management exp - Argentina, home-based Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We
Application Instructions: Please submit your resume in English when applying. Work Location Assignment: Buenos Aires, Argentina (Complejo LUMINA – Office Park). This role follows a hybrid model. Colleagues are expected to work from the assigned Pfizer
Application Instructions: Please submit your resume in English when applying. Work Location Assignment: Buenos Aires, Argentina (Complejo LUMINA – Office Park). This role follows a hybrid model. Colleagues are expected to work from the assigned Pfizer
As part of the Clinical Data Collection Strategies (CDCS) group, an integral delivery unit within the Clinical Development Information Sciences (CDIS) organization, the Database Analyst is responsible for the programming of high-quality clinical databases. Responsible for supporting
Work Location: Buenos Aires, Argentina (Complejo LUMINA – Office Park). This role follows a hybrid model; colleagues are expected to work from the assigned Pfizer office 2–3 days per week, or as required by business needs.
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
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)
# Associate Central Monitor, Data Surveillance, Clinical Data SciencesApplylocations: Argentina - Buenos Airestime type: Full timeposted on: Posted Todayjob requisition id: Application Instructions: Please submit your resume in English when applying. Work Location Assignment: Buenos Aires,
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
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
Study Lead Programmer - Argentina ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our