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5 дней назад

TIME Operations Manager (Clinical Trials)

65 000 - 100 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
middle
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
TIME Operations Manager (Clinical Trials): Managing the execution of clinical studies across the TIME network, from study start-up through closure, with an accent on pharmaceutical and CRO collaboration, regulatory compliance, and rapid site activation. Focus on coordinating complex trial deliverables, resolving operational risks, and accelerating cancer clinical trial completion through process and technology improvements.

Location: Remote - Illinois, United States; occasional travel required depending on the project.

Salary: $65,000–$100,000 annually.

Company

hirify.global develops a precision medicine platform that uses real-world evidence and AI to support clinical care and accelerate cancer clinical trials.

What you will do

  • Maintain and expand collaborations with pharmaceutical partners and CROs to support rapid study start-up.
  • Oversee study deliverables for assigned pharma clients, ensuring quality, timely execution, and customer satisfaction.
  • Manage studies within the TIME network from start-up through closure.
  • Prepare portfolios of trials for the network of research sites using clinical trial development and study start-up expertise.
  • Develop tactics, processes, tools, systems, and strategies to accelerate cancer clinical trial completion.
  • Collaborate with site operations, medical affairs, pathology, bioinformatics, and data science teams while identifying and resolving study risks.

Requirements

  • Bachelor’s degree and 4+ years of experience with complex clinical trials from a site, sponsor, or CRO perspective.
  • Advanced knowledge of FDA regulations, GCP, study start-up, clinical trial agreements, trial budgets, IRB submissions, and pharma operations.
  • Strong customer service, interpersonal, communication, and problem-solving skills.
  • Highly organized and systematic, with strong attention to detail and process improvement capabilities.
  • Ability to work independently and adapt in a fast-paced environment.
  • Must work remotely from Illinois, United States; occasional project-based travel is required.

Nice to have

  • Experience with rapid site activation.
  • Experience with research networks.
  • Clinical research project management experience.

Culture & Benefits

  • Full-time employment with a remote work arrangement.
  • Benefits may include incentive compensation, restricted stock units, medical coverage, and other benefits depending on the position.
  • Collaborative work across clinical, medical, pathology, bioinformatics, and data science functions.

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