6 дней назад
Patient Recruitment Specialist (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Patient Recruitment Specialist (Clinical Research): Supporting patient recruitment and retention activities for global clinical studies with an accent on study materials, country-specific documentation, timelines, and regulatory compliance. Focus on coordinating cross-functional stakeholders, tracking deliverables, maintaining accurate study data, and escalating operational risks.
Location: Sofia, Bulgaria
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Support patient recruitment and retention activities for assigned clinical studies.
- Coordinate the translation, production, and distribution of patient-facing and study materials.
- Prepare and manage country-specific submission packages and recruitment documentation.
- Track study timelines, milestones, deliverables, project reporting, and financial activities.
- Maintain accurate study data and documentation in designated systems and platforms.
- Collaborate with Regulatory, Clinical Operations, Project Management, Finance, and external vendors while identifying and escalating risks.
Requirements
- High school diploma or equivalent required; a bachelor's degree is preferred.
- Experience in clinical research, healthcare, life sciences, or project coordination is preferred.
- Knowledge of clinical trials and the drug development process is advantageous.
- Strong organizational skills, attention to detail, and the ability to manage multiple priorities.
- Proficiency with Microsoft Office applications, including Word and Excel.
- Fluent English and strong written and verbal communication skills.
Culture & Benefits
- Full-time employment supporting global clinical studies across multiple countries.
- Cross-functional collaboration with internal stakeholders, study teams, and external vendors.
- Work focused on compliant, accurate, and timely clinical study execution.
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