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Clinical programmer - cdmx

Johnson & Johnson
Publicada el 12 marzo
Descripción

At johnson & johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in innovative medicine and medtech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.as guided by our credo, johnson & johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At johnson & johnson, we respect the diversity and dignity of our employees and recognize their merit.job functiondata analytics & computational sciencesjob sub functionbiostatisticsjob categoryscientific/technologyall job posting locationsmexico city, mexicojob descriptionabout innovative medicineour expertise in innovative medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.learn more at https://www.jnj.com/innovative-medicineposition summarythe experienced programmer is an individual contributor with knowledge of data structures, industry standards, programming languages, and programming methods. This role supports data analyses and reporting activities within trial activities in accordance with departmental processes and procedures.this position is a member of the programming team, capable of supporting programming activities of one or more trials of low to medium complexity/criticality and may contribute to departmental innovation and process improvement projects.principal responsibilitiescompletes and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables.accountable for the design and development of programs in support of clinical research analysis and reporting.performs appropriate level of verification of programming and reporting activities. Reviews and provides input for project requirements and documentation.supports submission activities including but not limited to creation, verification, and delivery of cdisc compliant and/or non-standard data packages and reviewer’s guides.follows departmental processes and procedures, ensures use of latest standards and deployment of current technologies.may contribute to departmental innovation and process improvement projects.collaborates effectively with team and cross-functional members.ensures continued compliance with required company and departmental training, time reporting and other business/operational processes as required for position.clinical programmerreviews specifications for mapping internal data review model (drm) for fit-for-purpose reporting consumption and ensures verification of drm.supports data cleaning by programming edit checks and data review listings and data reporting by creating data visualizations and listings for data management, medical monitoring, and central monitoring.education and experience requirementsbachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical depth).experience and skills requiredapprox. 2+ years of relevant programming experience, preferably in pharmaceutical, cro or biotech industry or related field or industry.basic knowledge of regulatory guidelines (e.g. Ich-gcp) and relevant clinical r&d concepts.experience working in a team environment preferred.excellent written and verbal communications skills.knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting. May include sas, r, python, etc. Sas knowledge is preferred for clinical programming role.basic knowledge of processes, methods, and concepts relevant to programming.required skills(none listed)preferred skillsadvanced analyticsanalytical reasoningbiological sciencesbiostatisticsclinical trialsdata modelingdata privacy standardsdata qualitydata savvydetail-orientedgood clinical practice (gcp)report writingresearch ethicsresearchingstatistical analysis systems (sas) programmingstatisticstechnologically savvy
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