19 дней назад
Site Enablement Lead & Site Facing Line Manager (Clinical Research)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Site Enablement Lead & Site Facing Line Manager (Clinical Research): Leading the implementation and delivery of Site Enablement Solutions across clinical research sites in Turkey with an accent on site engagement, staff leadership, patient recruitment, and ICH-GCP compliance. Focus on building investigator and site relationships, improving service delivery and study outcomes, and supporting clinical research personnel across multiple priorities.
Location: Istanbul, Turkey; willingness to travel within Turkey is required.
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Lead the implementation and ongoing delivery of Site Enablement Solutions at clinical research sites.
- Build relationships with investigators, site personnel, and study teams to support study execution.
- Support the onboarding, development, performance, and engagement of site-based clinical research staff.
- Monitor service delivery, identify risks, and drive improvements in site performance and study outcomes.
- Provide training and operational support for site enablement tools and services.
- Collaborate with cross-functional stakeholders on quality, compliance, patient recruitment, and operational efficiency.
Requirements
- Bachelor’s degree in life sciences, healthcare, clinical research, business, or a related field.
- Experience in clinical research, site operations, patient recruitment, site management, or a similar environment.
- Direct experience working with clinical research sites, investigators, or site staff.
- Experience leading, coaching, mentoring, or managing personnel.
- Good understanding of clinical trial processes and ICH-GCP requirements.
- Fluency in Turkish and English, written and spoken, is required.
Nice to have
- Background as a Clinical Research Coordinator, Clinical Research Associate, Site Manager, Study Coordinator, or in a similar role.
- Experience supporting patient recruitment or site support services across multiple studies or sites.
- Clinical research certification such as CCRC or CCRP.
Culture & Benefits
- Opportunity to contribute to clinical research delivery and the development of treatments for patients.
- Work with industry-leading teams, innovative technologies, and a global healthcare and research network.
- Dynamic, matrixed environment focused on quality, compliance, operational excellence, and continuous improvement.
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