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2 дня назад

Senior Site Contracts Associate, IQVIA Biotech - Poland

151 200 - 374 100PLN
Формат работы
remote (только Poland)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Poland
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 Contracts Associate, IQVIA Biotech - Poland (clinical trial contracting): Managing contract strategy and start-up contracting activities for complex clinical studies and multi-protocol programs with an accent on investigator grant estimates, site agreements, regulatory compliance, and sponsor requirements. Focus on negotiating international contracts, building contracting processes and templates, tracking performance metrics, and mentoring colleagues.

Location: Poland - Homebased; the posting also lists Warsaw, Poland.

Salary: PLN 151,200–374,100 annualized base pay.

Company

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

What you will do

  • Develop investigator grant estimates, contracting strategies, proposal text, and contract or budget templates for complex studies.
  • Manage site agreements and start-up contracting activities, providing legal, operational, and financial expertise.
  • Collaborate with sponsors, stakeholders, and regional teams to deliver project scope and meet sponsor requirements.
  • Create and review scientific, technical, and administrative documentation for study initiation.
  • Track contracting performance, timelines, financial targets, and out-of-scope activities in CTMS and project systems.
  • Mentor colleagues, provide training, support quality standards, and act as a liaison for key clients.

Requirements

  • Bachelor’s degree in a related field.
  • 5+ years of site contracting experience within a sponsor or CRO, including international contract expertise.
  • Strong negotiation, communication, planning, organizational, and presentation skills.
  • Advanced legal, financial, and technical writing abilities.
  • Knowledge of clinical trial regulations, GCP/ICH, drug development, regulatory requirements, SOPs, and corporate standards.
  • Experience with clinical trial contract management, metrics, project leadership, and mentoring; strong Microsoft Office skills.

Culture & Benefits

  • Work on global, high-complexity clinical programs.
  • Collaborative, supportive, and growth-oriented work environment.
  • Opportunity to influence key clients and shape contracting strategy at scale.
  • Career progression and professional development opportunities.

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