Johnson & Johnson
Johnson & Johnson
Johnson & Johnson एक वैश्विक स्वास्थ्य सेवा कंपनी है, जो नवीन दवाओं और चिकित्सा प्रौद्योगिकी के क्षेत्र में काम करती है। इसकी टीमें ऑन्कोलॉजी, इम्यूनोलॉजी, न्यूरोसाइंस, विशेष नेत्र विज्ञान, इंटरवेंशनल केयर और ऑर्थोपेडिक्स में समाधान विकसित करती हैं तथा जटिल स्वास्थ्य आवश्यकताओं को पूरा करने के लिए विज्ञान और प्रौद्योगिकी का संयोजन करती हैं। दुनिया भर में स्वास्थ्य सेवा प्रदाताओं, मरीजों और समुदायों की सेवा करते हुए कंपनी स्वास्थ्य समानता, पर्यावरणीय स्थिरता, विविधता और समावेशन पर भी जोर देती है।

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.

विवरण

  • 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.

आवश्यकताएँ

  • 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.

लाभ

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

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