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6 дней назад

Patient Recruitment Specialist (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Bulgaria
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
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

hirify.global 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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