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4 дня назад

Research Project Coordinator (Clinical Trials)

Тип работы
fulltime
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
Research Project Coordinator (Clinical Trials): Coordinating the YouChoose Study evaluating self- and clinician-sampling options in NHS cervical screening, with an accent on clinical trial delivery, research governance, linked clinical data management, and regulatory compliance. Focus on maintaining the Trial Master File, coordinating data transfers with eight NHS laboratories, monitoring project risks and timelines, and supporting ethics and regulatory approvals.

Location: Oxford Road, based within the Division of Cancer Sciences at St Mary's Hospital, Manchester. Applicants must demonstrate the right to work in the UK; the role is not eligible for Skilled Worker visa sponsorship.

Company

hirify.global sponsors the YouChoose Study, an academic programme evaluating self- and clinician-sampling options in NHS cervical screening in England and Wales.

What you will do

  • Support the Project Manager with Trial Master File maintenance and project monitoring.
  • Coordinate confidential and efficient transfer of linked clinical data with eight NHS cervical screening laboratories.
  • Support adherence to the study protocol, research governance requirements, and regulatory guidelines.
  • Monitor delivery risks, update project plans, and track programme timelines and objectives.
  • Coordinate communication and engagement with university departments, other universities, NHS organisations, investigators, and collaborators.

Requirements

  • Biological science or social science degree at 2.2 or above, or equivalent research experience.
  • Experience supporting and managing research projects or clinical trials, preferably in an academic or NHS setting.
  • Experience coordinating clinical trials across research governance and delivery activities while meeting deadlines.
  • Excellent organisation skills and the ability to manage a varied workload.
  • Excellent oral and written communication skills in a multidisciplinary environment.

Nice to have

  • Good Clinical Practice training and understanding of research governance and ethical guidelines for work with humans or human tissue.
  • Experience with iProc or a similar electronic ordering system.
  • Experience organising and minuting meetings.
  • Experience producing progress reports for funding bodies, research ethics committees, and senior managers.

Culture & Benefits

  • Employer pension contribution.
  • Christmas closure across departments, outside annual leave and bank holidays.
  • Purple Place employee discount platform.
  • Inclusive environment supporting education, learning, community, diversity, and open discussion.

Hiring process

  • Applications close at midnight on the stated closing date.
  • Shortlisting and interviews are managed by the research team.

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