3 дня назад
Senior Project Manager (Clinical Trials)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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