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12 часов назад

Senior Site Contract Associate (Biotech)

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
France/Spain/Portugal +1 еще
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Senior Site Contract Associate (Biotech): Supporting clinical trial start-up contracting for biotech and emerging biopharma sponsors across multiple studies and therapeutic areas with an accent on contract negotiation, investigator budgets, regulatory compliance, and project delivery. Focus on interpreting pricing models, maintaining contracting systems, coordinating stakeholders, and ensuring accurate execution against timelines and financial goals.

Location: Homebased in France, Spain, Portugal or Greece

Company

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

What you will do

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

Requirements

  • Bachelor's degree in life sciences or healthcare.
  • More than 6 years of relevant experience, including demonstrable contract negotiation experience.
  • Experience in sponsor or clinical research organization site contracting.
  • Knowledge of regulated clinical trials, drug development, GCP/ICH and applicable regulatory requirements.
  • Strong negotiation, communication, technical writing, organization and planning skills.
  • Ability to interpret pricing models and prepare proposals, bid grids and budgets.

Culture & Benefits

  • Homebased work arrangement across France, Spain, Portugal and Greece.
  • Collaborative environment supporting clinical development for innovative treatments.
  • Work with biotech and emerging biopharma sponsors across multiple therapeutic areas.
  • Structured processes, project plans, contracting standards and operational support.

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