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Johnson & Johnson
Johnson & Johnson
Sponsor pentru viza H1BAsigurare de sănătateAsistență medicalăProduse farmaceutice
Johnson & Johnson este o companie globală din domeniul sănătății, care activează în medicina inovatoare și tehnologia medicală. Echipele sale dezvoltă soluții în oncologie, imunologie, neuroștiință, oftalmologie de specialitate, îngrijire intervențională și ortopedie, combinând știința și tehnologia pentru a răspunde unor nevoi complexe de sănătate. Compania pune, de asemenea, accent pe echitatea în sănătate, sustenabilitatea mediului, diversitate și incluziune, deservind furnizori de servicii medicale, pacienți și comunități din întreaga lume.
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Statistical Programmer, Clinical Research - Johnson & Johnson, Bangalore Hybrid

Support clinical trial programming, analyses, and CDISC-compliant submissions for Johnson & Johnson’s healthcare research programs. Develop R-based safety and reporting solutions while contributing to reliable clinical data deliverables.

INIndiaHibridNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăInginer software
Google Cloud PlatformPython

Descriere

  • Program and, where appropriate, lead low- to medium-complexity clinical trial activities while delivering accurate work on schedule.
  • Create and maintain programs for clinical research analyses and reporting.
  • Verify programming outputs and reporting activities using appropriate quality checks.
  • Review project requirements and contribute to supporting documentation.
  • Help prepare, verify, and deliver CDISC-compliant and non-standard data packages and reviewer guides for submissions.
  • Apply departmental procedures, current standards, and up-to-date technologies in daily programming work.
  • Participate in innovation initiatives and projects that improve departmental processes.
  • Work effectively with team members and cross-functional colleagues.
  • Complete required training, time reporting, and other company and departmental operational processes.
  • Report to a Delivery Unit people manager and remain accountable to Portfolio and Study Leads.
  • Coordinate with internal functional teams, external partners, CRO management, vendor liaisons, industry peers, and working groups.

Cerințe

  • Bachelor’s degree or higher, or equivalent expertise, in computer science, data science or engineering, mathematics, public health, or another relevant scientific discipline.
  • About two or more years of relevant programming experience, preferably in pharmaceuticals, CROs, biotechnology, or a related industry.
  • Basic familiarity with regulatory guidance such as ICH-GCP and with clinical research and development concepts.
  • Experience working collaboratively in a team setting is preferred.
  • Strong written and verbal communication skills.
  • Knowledge of data structures and programming languages used for data manipulation, statistical analysis, and reporting, including SAS, R, or Python.
  • Basic understanding of programming processes, methods, and concepts.
  • Experience with the R language and safety programming.
  • SAS knowledge is preferred for clinical programming work.

Beneficii

  • An inclusive workplace environment.
  • A culture that respects employee diversity and dignity.
  • Recognition for employee merit.

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ARArgentinaBOBoliviaBRBraziliaCLChileCOColumbiaCRCosta RicaCUCubaDORepublica DominicanăECEcuadorGTGuatemalaHNHondurasHTHaitiMXMexicNINicaraguaPAPanamaPEPeruPRPuerto RicoPYParaguaySVEl SalvadorUYUruguayVEVenezuelaRemoteNormă întreagăJuniorNu este necesară o diplomăLimbă Obligatorie: englezăLimbă Obligatorie: spaniolăTraducător

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