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12 дней назад

Global Study Associate Director - Single Sponsor Dedicated

Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
Spain
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Global Study Associate Director - Single Sponsor Dedicated (Clinical Research): Leading cross-functional clinical study teams and overseeing study delivery from handover through close-out, with an accent on timelines, budgets, quality standards, vendor coordination, and ICH-GCP compliance. Focus on managing study risks, maintaining inspection-ready documentation, overseeing Trial Master File completion, and driving communication with clinical program teams and external partners.

Location: Madrid, Spain

Company

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

What you will do

  • Lead cross-functional study teams and oversee outsourced clinical study delivery from handover through close-out and archiving.
  • Drive study milestones against agreed timelines, budgets, quality standards, and operational KPIs.
  • Coordinate communication with Clinical Program Teams, internal functions, investigators, CROs, laboratories, and other external service providers.
  • Oversee study-level documents, plans, risk management, vendor performance, Trial Master File completion, and inspection readiness.
  • Manage study budgets, re-forecasting, change control, financial risk reporting, and mitigation planning.
  • Identify quality issues, coordinate corrective action plans, provide team feedback, and contribute to process improvement initiatives.

Requirements

  • University degree or equivalent, preferably in medical or biological sciences or a clinical research-related discipline.
  • At least 5 years of relevant clinical experience in the pharmaceutical industry, including 2 years of project management experience, or an equivalent combination of education, training, and experience.
  • Extensive knowledge of ICH-GCP, clinical research regulations, clinical study management, and clinical or drug development processes.
  • Demonstrated project management, team leadership, communication, conflict management, strategic thinking, organizational, and problem-solving skills.
  • Ability to manage competing priorities and maintain effective relationships with internal and external stakeholders.

Culture & Benefits

  • Work within a global organization focused on accelerating the development and commercialization of medical treatments.
  • Opportunity to contribute to healthcare and life sciences research that supports improved patient outcomes and population health.
  • Inclusive workplace focused on diversity, equality, belonging, and collaboration.

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