5 дней назад
Senior Global Study Manager (Central Lab Services)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Global Study Manager (Central Lab Services): Managing complex global clinical studies and client deliverables for Central Lab Services with an accent on stakeholder communication, budget, risk, timeline, and regulatory management. Focus on leading cross-functional teams, solving delivery challenges, and driving process improvement across clinical trial projects.
Location: Fully remote in Bulgaria; listed location: Sofia, Bulgaria.
Company
provides laboratory and drug development services supporting pharmaceutical, biotechnology, healthcare, and clinical research organizations.
What you will do
- Act as the primary client contact and coordinate communication between clients, CROs, , and extended study teams.
- Manage a portfolio of complex global clinical studies within Central Lab Services.
- Oversee client deliverables, budgets, risks, milestones, performance metrics, and reporting.
- Review statements of work and ensure client requirements are implemented accurately and in compliance with regulatory requirements.
- Lead cross-functional collaboration, remove roadblocks, and maintain delivery quality, timelines, and productivity.
- Drive continuous improvement, process updates, and operational excellence across clinical project management activities.
Requirements
- Bachelor’s degree.
- At least 5 years of experience in the pharmaceutical, biotechnology, or CRO industry.
- At least 5 years of experience managing complex global clinical projects, including budgets, risks, timelines, and stakeholders.
- At least 5 years of client-facing and stakeholder management experience.
- At least 2 years of Central Labs experience.
- Strong knowledge of clinical trials, project management methodologies, clinical development processes, leadership, strategic thinking, and independent decision-making.
Nice to have
- Master’s or other university degree.
- Project management training or certification such as PMP or PRINCE2.
Culture & Benefits
- Fully remote work arrangement with a Monday–Friday schedule.
- Opportunity to support clinical trials and drug development across global teams.
- Mentoring, training, and personalized development planning.
- Focus on inclusion, continuous improvement, quality, productivity, and exceptional client service.
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