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🚀 Internship

Clinical Trial Internship - 12 Months

Logo of Perspectum Ltd

Perspectum Ltd

11d ago

🚀 Placement Program


🤑 £22K - £22K
16hrs left

AI generated summary

  • Keen interest and knowledge in clinical trials, exceptional organization and communication skills, attention to detail, ability to work independently and collaboratively, strong time management, proficiency in IT, efficient documentation management.
  • The Clinical Trial Intern will be responsible for coordinating study meetings, tracking participant visits and expenses, managing study documentation and data systems, monitoring study progression, and supporting site initiation and feasibility assessments.

Placement Program



  • As Clinical Trial Intern, you'll be pivotal in supporting our team's day-to-day activities related to Perspectum's studies. We're looking for someone who can tackle challenges with a proactive and independent mindset, contributing to our mission of advancing healthcare through innovation.


  • You will have a keen interest in Clinical trials and have either studied, worked or have some knowledge within a similar industry.
  • Strong self-motivation and exceptional organisation.
  • Outstanding communication.
  • Impeccable attention to detail and commitment to quality.
  • Able to work autonomously as well as collaboratively within a team.
  • Effective time management, consistently meeting deadlines.
  • Proficiency in IT, particularly with O365.
  • Ability to efficiently manage and coordinate the creation and delivery of documentation on schedule.

Education requirements

Currently Studying

Area of Responsibilities



  • Drafting, revising, and flagging study documentation for necessary updates.
  • Planning and coordinating both on-site and off-site study meetings, including collating supporting materials and circulating agendas
  • Tracking study participant visits, expenses, invoices, and payments.
  • Producing and maintaining clear and concise meeting minutes, ensuring follow-up on action items.
  • Coordinating regular updates on project milestones and deliverables.
  • Managing and monitoring Electronic Data Capture, Clinical Trial Management System, and Investigator Site File.
  • Monitoring study progression against established timelines.
  • Ensuring effective cross-team communication and coordination.
  • Supporting study start-up activities, including site initiation visits.
  • Evaluating and coordinating site feasibility and setup
  • Conducting study feasibility assessments.


Work type

Full time

Work mode


Application deadline

Feb 23, 2024




22000 - 22000 GBP