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Thermo Fisher Scientific
Thermo Fisher Scientific
H1B vizos rėmėjasGamybaLogistikaSveikatos priežiūra
„Thermo Fisher Scientific“ kuria ir tiekia technologijas, laboratorijų produktus bei farmacijos paslaugas, padedančias vykdyti mokslinius tyrimus ir teikti sveikatos priežiūrą. Įmonės veikla apima gyvybės mokslų tyrimus, analitinių problemų sprendimą, laboratorijų našumo didinimą, diagnostiką, taip pat gydymo metodų kūrimą ir gamybą. Klientams visame pasaulyje ji teikia paslaugas pasitelkdama tarptautinę komandą ir prekių ženklų portfelį, kurį sudaro „Thermo Scientific“, „Applied Biosystems“, „Invitrogen“, „Fisher Scientific“, „Unity Lab Services“, „Patheon“ ir „PPD“. Įmonės karjeros galimybės apima su šiais pasiūlymais susijusias mokslo, sveikatos priežiūros, gamybos, logistikos ir paslaugų veiklas.
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Remote Clinical Trial Contract Specialist – Argentina

Negotiate clinical trial site agreements, investigator budgets, and legal terms for Thermo Fisher Scientific. Coordinate with study startup teams to support site activation across international trials.

ARArgentinaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųBendraSutarčių specialistas

Aprašymas

  • Prepare, review, negotiate, and complete agreements with clinical study sites.
  • Negotiate investigator grant budgets and contract terms within approved limits.
  • Follow negotiation guidelines, delegated approval authority, contract processes, client needs, budget guidance, templates, and established procedures.
  • Evaluate legal, financial, and operational risks, escalating concerns when needed.
  • Recommend options and alternative solutions during investigator contract negotiations.
  • Work with internal teams on site startup and contract activities, coordinating agreed timelines.
  • Keep contract negotiations on the critical path to site activation.
  • Meet site activation cycle time targets.
  • Route issues outside approved parameters through established escalation channels.

Reikalavimai

  • Bachelor’s degree or equivalent, with relevant formal academic or vocational qualifications.
  • 2–5 years of relevant prior experience.
  • Strong spoken and written communication skills in English and the local language.
  • A sound understanding of contract law, including business, intellectual property, local tax, and stamp laws.
  • Ability to apply basic investigator grant negotiation principles.
  • General knowledge of business and financial principles related to service agreements.
  • Ability to draft and negotiate contract clauses and budget matters within approved limits.
  • Careful attention to detail.
  • Strong analytical and decision-making skills.
  • Understanding of pharmaceutical product development and CRO involvement.
  • Ability to work independently and collaboratively.
  • Good organizational and time management skills.
  • Working knowledge of PPD SOPs and WPDs.
  • Ability to manage competing priorities and assess contractual risks and issues.
  • Proficiency with automated systems and computer applications.
  • Customer-focused communication, problem-solving, and collaboration skills.
  • Ability to remain upright and/or stationary for 6–8 hours per day.
  • Ability to perform repetitive hand movements and move frequently.
  • Ability to lift and carry objects, luggage, and a laptop weighing up to 15–20 lbs.
  • Regular and consistent attendance.
  • Ability to manage stress and multitask.

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