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GSK
GSK
H1B vizasi homiysiFarmatsevtika mahsulotlariIshlab chiqarishSog‘liqni saqlash
GSK dori vositalari va vaksinalarni ishlab chiqish uchun ilmiy tadqiqotlar, texnologiya hamda soha bo‘yicha ixtisoslashgan mutaxassislarni birlashtiradigan global sog‘liqni saqlash va farmatsevtika kompaniyasidir. Uning faoliyati kasalliklarning oldini olish va ularni boshqarishga yordam berishga mo‘ljallangan mahsulotlarni kashf etish, ishlab chiqarish va yetkazib berishni qamrab oladi. Kompaniya yirik xalqaro tashkilotda sog‘liqni saqlash sohasidagi innovatsiyalarga hissa qo‘shish imkonini beradi.
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Kompaniyadagi ish o‘rinlari

Principal Clinical Programmer

Lead clinical trial programming, analysis packages and regulatory support at GSK. Mentor programmers and uphold CDISC-compliant quality across pivotal studies.

USAmerika Qo‘shma ShtatlariMAMassachusetsPAPensilvaniya
126 225 $ – 210 375 $ / yil
GibridTo‘liq stavkaYetakchiTalab Qilinadigan Til: inglizchaDasturiy ta’minot muhandisi
Python

Tavsif

  • Lead programming activities independently across one or more studies.
  • Develop, maintain and validate complex analysis packages.
  • Maintain quality assurance by following Good Programming Practices and CDISC standards.
  • Guide junior programmers in technical methods and industry best practices.
  • Provide programming support for EMA and FDA regulatory interactions.
  • Identify gaps and inefficiencies, then implement practical improvements aligned with standards and best practices.
  • Set up and maintain governance frameworks.
  • Spot risks early, plan mitigations and escalate issues promptly.
  • Work with clinical, statistical and operational stakeholders.
  • Translate scientific needs into technical solutions for clinical development programmes.

Talablar

  • At least five years of programming experience in pharmaceuticals, biotechnology, healthcare or another regulated industry.
  • Experience programming in SAS, R, Python or a comparable language.
  • Experience supporting clinical trials or development programmes, or analyzing clinical research data.
  • Experience developing, validating and maintaining custom programs, analyses, tables, figures or listings.
  • Experience applying programming standards, quality controls and regulatory requirements in a regulated environment.
  • Expertise in oncology-specific requirements, such as RECIST 1.1.
  • Experience working with cross-functional stakeholders to deliver programming or data analysis solutions.
  • Experience guiding others in using AI/ML tools or applying them to improve efficiency.
  • Experience contributing to internal technical discussions, forums or external technical organizations.
  • Experience contributing to department strategies and technical initiatives through working groups or subteams.
  • Demonstrated collaboration and networking across departments, divisions and external partners.
  • Experience coordinating work across matrix teams and contributing to programming plans and execution.
  • Experience guiding teams and individuals while promoting continuous improvement, collaboration and innovation.
  • Strong expertise in applying CDISC standards.
  • Demonstrated proficiency in R.

Imtiyozlar

  • Competitive salary.
  • Annual bonus linked to company performance.
  • Healthcare and wellbeing programmes.
  • Pension plan membership.
  • Shares and savings programme.
  • Hybrid working, combining remote and office work.
  • Health care and other insurance coverage for employees and their families.
  • Retirement benefits.
  • Paid holidays.
  • Vacation.
  • Paid caregiver, parental and medical leave.
  • Eligibility for a share-based long-term incentive programme.

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