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1 день назад

Sr. Site Activation Specialist, Contract Negotiator (Clinical Research)

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Romania
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
Sr. Site Activation Specialist, Contract Negotiator (Clinical Research): Managing clinical trial site activation, Clinical Trial Agreement negotiations, and site budgets in Romania with an accent on contract execution, regulatory compliance, and cross-functional coordination. Focus on negotiating legal and financial terms, preparing CTA amendments, improving start-up timelines, and maintaining accurate contract documentation.

Location: Bucharest, Romania; hybrid work model

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead the negotiation and ongoing management of Clinical Trial Agreements with investigative sites and investigators.
  • Review and negotiate site budgets based on sponsor calculations and study requirements.
  • Coordinate with Clinical and RSU teams to support timely site start-up and forecast contract execution timelines.
  • Explain legal and financial terms to internal and external stakeholders and prepare CTA amendments.
  • Perform contract quality control and maintain accurate, complete, compliant documentation and archives.
  • Participate in project meetings and contribute to process improvements and operational efficiency.

Requirements

  • Bachelor’s degree in Life Sciences, Legal Studies, or a related field.
  • At least 3 years of clinical research experience, or an equivalent combination of education, training, and experience.
  • Experience with site activation, study start-up, and CTA negotiation is highly preferred.
  • Advanced English proficiency and native Romanian language skills are required.
  • Strong communication, stakeholder management, negotiation, problem-solving, organizational, and prioritization skills.
  • Ability to work cross-functionally and take ownership under moderate supervision.

Nice to have

  • Knowledge of clinical trial systems.
  • Regulatory experience, including document preparation and CTIS submissions.
  • Legal background.

Culture & Benefits

  • Collaborative environment within a global organization.
  • Opportunity to contribute to clinical research projects.
  • Professional development across site activation and contract management.

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