12 дней назад
Global Study Associate Director - Single Sponsor Dedicated
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →