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3 дня назад

Senior Project Manager (Clinical Trials)

Формат работы
remote (только Romania)
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Romania
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
Senior Project Manager (Clinical Trials): Leading complex clinical trials for pharmaceutical, biotechnology, medical device, and consumer health clients with an accent on cross-functional delivery, sponsor coordination, regulatory compliance, timelines, and budgets. Focus on managing CRO-based study operations, coordinating clinical research teams, overseeing documentation and approvals, and supporting respiratory, rare disease, general medicine, or GLP-1 studies.

Location: Permanent remote opportunity in Romania

Company

hirify.global is a global full-service CRO providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

  • Lead and coordinate complex clinical projects, cross-functional teams, sponsors, investigators, and clinical research personnel.
  • Oversee study services, documentation, data collection, regulatory activities, archiving, and project-specific deliverables.
  • Manage project timelines, budgets, workload, team performance, risks, and sponsor updates.
  • Coordinate Clinical Research Associates, Clinical Monitors, Clinical Trial Administrators, Biometrics, Safety, and Regulatory functions.
  • Support protocols, Case Report Forms, Clinical Study Reports, SOPs, training, and Monitor or Investigator Meetings.
  • Perform co-monitoring visits and mentor Project Coordinators and Project Manager I staff when required.

Requirements

  • Must be based in Romania for this permanent remote role.
  • At least 8 years of clinical research project management experience and previous CRO experience are required.
  • Experience managing respiratory, rare disease, general medicine, and/or GLP-1 studies is required.
  • Bachelor's degree or equivalent in a scientific, medical, paramedical, or nursing discipline.
  • Strong knowledge of clinical trial operations, GCP/ICH guidelines, and applicable regulatory requirements.
  • Fluent English is required. Proficiency in Microsoft Office is also required.

Nice to have

  • Previous Clinical Research Associate or Clinical Monitor experience.
  • Experience with electronic data capture systems.
  • Experience acting as a Technical Specialist in a therapeutic or technical area.

Culture & Benefits

  • Permanent remote work from Romania.
  • Collaborative, quality-driven one-team culture.
  • Professional development and continuous training programs.
  • Work supporting pharmaceutical, biotechnology, medical device, and consumer health projects.
  • Equal opportunity workplace focused on diversity and inclusion.

Hiring process

  • Submit a CV and receive an application acknowledgement.
  • Qualified candidates are invited to a phone interview as the first step.

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