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2 дня назад

Senior Site Contracts Associate (Clinical Trials)

Формат работы
remote (только Germany)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Germany
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 (Clinical Trials): Managing contract strategy and site start-up contracting activities for complex international clinical studies and multi-protocol programs with an accent on investigator grant estimates, negotiation, regulatory compliance, and contracting performance. Focus on developing contracting strategies, coordinating sponsors and regional teams, mentoring colleagues, and maintaining efficient delivery against timelines and financial targets.

Location: Home-based in Germany; the posting also lists Frankfurt, Hesse, Germany.

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, and proposal content for complex studies.
  • Create and maintain contract and budget templates, systems, tools, processes, and training materials.
  • Manage site agreements and start-up contracting activities, providing legal, operational, and financial expertise.
  • Coordinate with sponsors, stakeholders, and regional teams to deliver project scope and meet sponsor requirements.
  • Track contracting metrics, timelines, financial targets, and out-of-scope activities while maintaining CTMS and project documentation.
  • Mentor and coach colleagues, provide technical guidance, and represent contracting activities to clients and professional bodies.

Requirements

  • Bachelor’s degree in a related field or an equivalent combination of education, training, and experience.
  • At least 5 years of site contracting experience within a sponsor or CRO, including international contract expertise.
  • Strong negotiation, communication, interpersonal, planning, organizational, and presentation skills.
  • Advanced legal, financial, and technical writing abilities, with a strong understanding of clinical trial regulations, GCP/ICH, drug development, SOPs, and regulatory requirements.
  • Experience with project leadership, mentoring, matrix teams, contracting metrics, and complex contract management processes.
  • Strong proficiency in Microsoft Word, Excel, and other Microsoft Office tools.

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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