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Thermo Fisher Scientific
Thermo Fisher Scientific
H1B vīzas sponsorsLoģistikaRažošanaVeselības aprūpe
Thermo Fisher Scientific izstrādā un piegādā tehnoloģijas, laboratoriju produktus un farmācijas pakalpojumus, kas atbalsta zinātnisko pētniecību un veselības aprūpi. Uzņēmuma darbība aptver dzīvības zinātņu pētniecību, analītisko problēmu risināšanu, laboratoriju darba ražīgumu, diagnostiku, kā arī terapiju izstrādi un ražošanu. Uzņēmums apkalpo klientus ar globālas komandas un zīmolu portfeļa palīdzību, kurā ietilpst Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon un PPD. Uzņēmuma karjeras iespējas aptver zinātnes, veselības aprūpes, ražošanas, loģistikas un pakalpojumu darbības, kas nodrošina šos piedāvājumus.
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Vakances uzņēmumā

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.

ARArgentīnaAttālinātiPilna slodzeJaunākais speciālistsVidējais līmenisNepieciešamā Valoda: angļuLīgumu speciālistsVispārīgi

Apraksts

  • 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.

Prasības

  • 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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