1 месяц назад
Clinical Research Associate 1/2 - Czech Republic
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Research Associate 1/2 - Czech Republic (Clinical Trials): Performing site selection, initiation, monitoring, and close-out visits while tracking recruitment, regulatory submissions, case report forms, and data queries with an accent on Good Clinical Practice, site quality, and clinical trial integrity. Focus on coordinating study progress, collaborating with sites and client representatives, and managing monitoring activities across therapeutic areas.
Location: Prague, Czech Republic
Company
IQVIA provides 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 in line with regulatory requirements, Good Clinical Practice, and ICH 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.
- Experience in the pharmaceutical industry and/or clinical trials.
- Excellent command of Czech and English.
- Very good computer skills, including MS Office.
- Organizational, time-management, problem-solving, and relationship-building skills.
- Flexibility to travel and a Class B driver's license.
Culture & Benefits
- Career-growth resources and programs for building therapeutic knowledge.
- Flexible work schedules supported by leaders.
- International and reputable working environment.
- Mobile phone and an attractive benefits package.
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