Назад
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13 дней назад

Sr. Clinical Project Manager (MedTech)

93 100 - 232 800$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
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
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

hirify.global 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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