Senior Data Lead - Argentina - Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility,
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
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
Job Overview Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis, formulate recommendations
Job Description The Associate Director, Global Data Management and Standards - Business Operation, is responsible for collaborating with the teams Leadership to drive enterprise-wide planning, governance, and organizational readiness initiatives that enable successful execution of strategic
Job Description The Associate Director, Data Architect (M-track) leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to leadership and partners. Provide
Job Overview Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis, formulate recommendations
EDETEK is seeking an experienced and highly motivated Senior Clinical Project Manager to lead the planning, execution, and oversight of clinical trials for pharmaceutical, biotechnology, and medical device clients. This role is responsible for cross-functional project leadership from
We are seeking a senior QA specialist who will play a critical role in driving compliance and quality across the organization’s biometric services and computer systems. This role involves hands-on execution of QA activities, leadership in
Senior Data Lead - Argentina - Remote 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
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.
Parexel FSP is looking for a Clinical Laboratory Study Manager. The candidate can be based anywhere in Argentina, Brazil, and/or Mexico. The Clinical Laboratory Study Manager works closely with Precision Medicine Leadership and cross-functional study teams (i.e. clinical, data
Senior Data Lead - Argentina - Remote 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
Parexel International is seeking a Clinical Laboratory Study Manager who can work from anywhere in Argentina, Brazil, or Mexico. This role involves managing high-quality samples and data, supporting precision medicine strategies, and overseeing clinical trial supplies. The ideal
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.
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,
The Senior Pricing and Proposal Specialist, Biometrics is responsible for developing competitive, accurate, and commercially sound budgets, proposals, assumptions, and supporting materials for biometrics-related opportunities, including Biostatistics, Statistical Programming, Clinical Data Management, PK/PD, Medical Writing support, and related
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 Description We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team. Please note the official PSI CRO job title will be: Senior Database Developer. If you are
Job Overview Under broad guidance, performs activities related to the analysis, design, programming, debugging, modification, and maintenance of software enhancements and/or new products. Essential Functions • Under broad guidance, analyzes, designs, programs, debugs, modifies, and maintains software