13 дней назад
Sr. Clinical Project Manager (MedTech)
93 100 - 232 800$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Sr. Clinical Project Manager (MedTech): Leading the planning, execution, and delivery of global medical device clinical studies with an accent on sponsor management, cross-functional leadership, regulatory compliance, and financial performance. Focus on managing multi-country programs, resolving project risks, supporting regulatory submissions, and driving operational excellence across clinical study teams.
Location: Washington, DC, United States of America
Salary: $93,100–$232,800 annual base pay
Company
provides clinical research services, commercial insights, and healthcare intelligence for life sciences and healthcare organizations.
What you will do
- Lead the planning, execution, and delivery of global and multi-country MedTech clinical studies.
- Act as the primary contact for sponsors and maintain client relationships throughout the study lifecycle.
- Manage study timelines, budgets, forecasts, risks, deliverables, scope changes, and project profitability.
- Lead cross-functional teams and collaborate with Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Safety, and other functions.
- Monitor progress, resolve issues, provide strategic updates, and ensure milestones and study objectives are achieved.
- Support bid defenses, continuous improvement, knowledge sharing, and the development of junior project management and clinical operations staff.
Requirements
- Bachelor’s degree in Life Sciences, Nursing, Biomedical Engineering, Public Health, Healthcare, or a related scientific discipline.
- At least 7 years of clinical research experience, including 4 years of clinical project management experience.
- Experience in MedTech, medical devices, diagnostics, CRO, biotechnology, pharmaceutical, or healthcare environments.
- Experience leading global and multi-country studies across North America, Europe, Asia-Pacific, and other regions.
- Knowledge of clinical trial management, ICH-GCP, ISO 14155, FDA, global regulatory requirements, SOPs, and quality standards.
- Strong project planning, stakeholder management, communication, negotiation, budgeting, forecasting, and problem-solving skills.
Nice to have
- Experience supporting regulatory submissions, product development, or post-market evidence generation.
Culture & Benefits
- Work in a global, cross-functional, matrix environment.
- Focus on customer service, operational excellence, quality, and continuous improvement.
- Health and welfare benefits may be provided in addition to base pay.
- Incentive plans, bonuses, or other compensation may be available depending on the position.
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