Johnson & Johnson
Johnson & Johnson
Johnson & Johnson innovatsion dori vositalari va tibbiy texnologiyalar yo‘nalishlarida faoliyat yurituvchi global sog‘liqni saqlash kompaniyasidir. Uning jamoalari onkologiya, immunologiya, nevrologiya, maxsus oftalmologiya, intervensional tibbiyot va ortopediya sohalarida yechimlar ishlab chiqib, murakkab tibbiy ehtiyojlarni hal etish uchun fan va texnologiyani birlashtiradi. Kompaniya butun dunyo bo‘ylab tibbiyot xodimlari, bemorlar va jamoalarga xizmat ko‘rsatish bilan birga, sog‘liqni saqlashda tenglik, ekologik barqarorlik, xilma-xillik va inklyuzivlikka ham katta e’tibor qaratadi.

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.

Tavsif

  • 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.

Talablar

  • 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.

Imtiyozlar

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

O‘xshash ish o‘rinlari

Kreato Global | BPO and Language Solutions

Remote English-Spanish OPI/VRI Interpreter

Kreato Global | BPO and Language Solutions

Interpret remotely between English- and Spanish-speaking people in medical, financial, social service, and customer care settings. Provide language support for Kreato Global across Latin America.

Ochish
RecruitGo

Remote Executive Assistant, Outreach and Marketing — Philippines

RecruitGo
51 – 200 Xodimlar
KonsaltingLogistikaMarketing

Handle administrative support, CRM, outreach, and marketing for RecruitGo, an Employer of Record serving global clients with talent from emerging markets. Support two UK-facing clients with day-to-day administration and creative campaigns.

Ochish