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11 дней назад

Manager Flexible Resourcing, Sponsor Dedicated in Türkiye (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Turkey
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
Manager Flexible Resourcing, Sponsor Dedicated in Türkiye (Clinical Research) (Clinical Research): Managing a team of CRAs/SrCRAs and allocating clinical research staff to studies for a dedicated pharmaceutical sponsor with an accent on team leadership, resource planning, and clinical work quality. Focus on identifying quality risks, creating action plans, monitoring performance metrics, and supporting professional development.

Location: Istanbul, Turkey

Company

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

What you will do

  • Manage a team of CRAs, Senior CRAs, and potentially CTAs in a sponsor-dedicated setting for one pharmaceutical client.
  • Plan, assign, and direct work while evaluating performance, supporting professional development, and resolving employee relations issues.
  • Participate in recruitment, interviews, onboarding, training, and preparation of systems and materials for new team members.
  • Allocate staff to clinical studies based on study requirements, experience, and training.
  • Review clinical work quality, identify risks, and develop appropriate action plans.
  • Monitor task completion and quality metrics, regularly reviewing and reporting findings to clinical operations management.

Requirements

  • University degree in a scientific or healthcare discipline, or an equivalent combination of education, training, and experience.
  • Several years of clinical research experience, including leadership experience.
  • Fluent Turkish and good command of English; candidates must be based in Türkiye.
  • Strong organizational, interpersonal, teamwork, leadership, and problem-solving skills.
  • Ability to manage multiple priorities, meet deadlines, and maintain attention to detail and accuracy.
  • Proficiency in Microsoft tools.

Culture & Benefits

  • Work in close partnership with a key pharmaceutical sponsor.
  • Participate in clinical trial projects within a Clinical Functional Service Partnership team.
  • Collaborate with sponsor representatives and clinical operations stakeholders.

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