1 месяц назад
Experienced Clinical Research Associate (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Experienced Clinical Research Associate (Clinical Research): Performing site selection, initiation, monitoring, and close-out visits for clinical studies with an accent on Good Clinical Practice compliance, recruitment planning, and regulatory tracking. Focus on evaluating site quality, resolving data queries, coordinating study progress, and collaborating with study-site experts and client representatives.
Location: Prague, Czech Republic; candidates must be based in the Czech Republic
Company
Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Perform site selection, initiation, monitoring, and close-out visits.
- Support the development of subject recruitment plans.
- Evaluate site practices for quality and integrity against regulatory requirements, Good Clinical Practice, and International Conference on Harmonization guidelines.
- Track regulatory submissions, recruitment, case report form completion, and data query resolution.
- Collaborate with study-site experts and client representatives.
Requirements
- University degree in a scientific discipline or healthcare.
- At least two years of experience as a Clinical Research Associate.
- Excellent command of Czech and English; Czech Republic-based.
- Very good computer skills, including MS Office.
- Strong organizational, time-management, problem-solving, and relationship-building skills.
- Flexibility to travel and a class B driver's license.
Culture & Benefits
- Resources and programs supporting career growth and therapeutic knowledge development.
- Flexible work schedules supported by leadership.
- International and reputable working environment.
- Company car, mobile phone, and benefits package.
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