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GSK
GSK
Sponzor vizuma H1BFarmacevtski izdelkiProizvodnjaZdravstveno varstvo
GSK je globalno zdravstveno in farmacevtsko podjetje, ki združuje znanstvene raziskave, tehnologijo in specializirane strokovnjake za razvoj zdravil in cepiv. Njegovo delo obsega odkrivanje, proizvodnjo in dostavo izdelkov, namenjenih preprečevanju in obvladovanju bolezni, ter ponuja priložnosti za prispevanje k inovacijam v zdravstvu znotraj velike mednarodne organizacije.
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Delovna mesta v podjetju

Principal Clinical Programmer

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

USZdružene države AmerikeMAMassachusettsPAPensilvanija
126.225 $ – 210.375 $ / leto
HibridnoPolni delovni časVodjaZahtevani Jezik: angleščinaProgramski inženir
Python

Opis

  • 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.

Zahteve

  • 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.

Ugodnosti

  • 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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