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12 часов назад

Clinical Trials Scientific Affairs Supervisor

Формат работы
remote (только United_kingdom)
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
UK
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
Clinical Trials Scientific Affairs Supervisor (Clinical Trials/Scientific Affairs): Managing pre-award clinical trial testing reviews, referral laboratory coordination, pricing documents, and scientific responses for RFPs and RFIs with an accent on team leadership, regulated laboratory operations, and cross-functional delivery. Focus on determining protocol testing requirements, coordinating referral laboratories, improving operational processes, and resolving study-related testing issues.

Location: Remote, United Kingdom

Company

hirify.global provides laboratory and scientific services supporting clinical trials and regulated testing activities.

What you will do

  • Manage daily department performance, resources, workload prioritization, staffing capacity, and operational metrics.
  • Lead, coach, train, and develop direct reports, including onboarding, performance management, and career development.
  • Review clinical trial protocols to determine testing requirements, testing facilities, methods, and associated referral laboratory needs.
  • Prepare and review pricing documents and provide scientific and technical information for client RFPs and RFIs.
  • Coordinate with Commercial, Operations, Scientific, Sales, HR, referral laboratories, and external clients to resolve study and testing issues.
  • Lead process improvements, update SOPs, maintain templates and tools, and support root cause analysis and operational efficiency.

Requirements

  • Must be based in the United Kingdom while working remotely.
  • Bachelor’s degree in a relevant scientific discipline or at least 3 years of experience as a Clinical Laboratory Scientist.
  • At least 5 years of laboratory experience in a clinical setting or relevant regulated environment.
  • Strong interpersonal, communication, time-management, organizational, and multitasking skills.
  • Ability to work independently and collaboratively, lead and motivate others, and manage projects with tight deadlines.
  • Proficiency in Microsoft Office and respect for patient confidentiality and company procedures.

Nice to have

  • Generalist laboratory experience.
  • MT (ASCP) certification.
  • A positive, solutions-oriented mindset.

Culture & Benefits

  • Full-time schedule of 37.5 hours per week, Monday through Friday during daytime hours.
  • Remote work arrangement within the United Kingdom.
  • Work involving cross-functional collaboration, continuous education, coaching, and professional development.
  • Sedentary, primarily office-based role requiring prolonged computer work and sustained concentration.
  • Some roles may require flexible hours, TB screening, or a valid driver’s license.

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