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2 дня назад

Senior Site Contract Associate - IQVIA Biotech

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Serbia/CR
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Site Contract Associate - IQVIA Biotech (Clinical Trial Contracting): Supporting start-up contracting activities, investigator grant estimates, proposal development, and contract management for biotech clinical trials with an accent on sponsor collaboration, regulatory compliance, and financial accuracy. Focus on negotiating site contracts, maintaining budgets and contracting systems, and ensuring study initiation activities meet project timelines and quality standards.

Location: Homebased in Serbia or the Czech Republic

Company

IQVIA Biotech supports biotech and emerging biopharma companies with clinical development services across therapeutic areas and development phases.

What you will do

  • Support start-up contracting activities for sponsors, clinical studies, and multi-protocol programs, including pre-award work.
  • Prepare investigator grant estimates, proposal text, pricing models, bid grids, and budgets.
  • Maintain contract and budget templates, contracting systems, CTMS data, tracking tools, timelines, and project plans.
  • Collaborate with sponsors, stakeholders, and regional and country teams to deliver contracted project scope.
  • Provide operational and financial contracting support for clinical trial initiation and maintenance.
  • Track contracting performance, support quality standards, and report timeline, financial, and out-of-scope activities.

Requirements

  • Bachelor’s degree in life sciences or healthcare.
  • 5–7 years of relevant experience, including demonstrable contract negotiation experience.
  • Experience in clinical site contracting within a sponsor or clinical research organization.
  • Knowledge of the regulated clinical trial environment, drug development processes, GCP/ICH, applicable regulations, SOPs, and corporate standards.
  • Strong negotiation, communication, technical writing, organization, planning, and interpersonal skills.
  • Strong knowledge of Microsoft Office and email applications, plus the ability to interpret pricing models and manage clinical trial contracts.

Culture & Benefits

  • Home-based work arrangement in Serbia or the Czech Republic.
  • Collaboration with biotech and emerging biopharma sponsors across clinical development programs.
  • Work within an agile and collaborative structure focused on clinical research and healthcare innovation.

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