Clinical Trial Manager

3 weeks ago

London, Greater London, United Kingdom Imperial College London Full time

An exciting opportunity has arisen for a Clinical Trial Manager to work in a research unit at Imperial College London.

The post holder will oversee an NIHR funded multi-centred randomised clinical trial within the academic section of surgery portfolio. The Spinal Injury Study randomises 8000 patients to receive either triple immobilisation (standard of care) or movement minimisation in the pre-hospital phase. This study is sponsored by Imperial College working with Warwick CTU. You will be responsible for all aspects of trial management, including close liaison with the Chief Investigator and PIs at other centres, management of the associated study staff and implementing / adapting established systems and processes to ensure the trial is developed and conducted to the highest scientific and regulatory standards. Our role in the study is the recruitment and management of study sites and follow up of patients recruited once out of hospital.

The post holder will be responsible for managing the day-to-day activities of the trial, including the coordination of study staff, the management of study sites, and the implementation of trial protocols. You will also be responsible for ensuring that the trial is conducted in accordance with the highest scientific and regulatory standards, and that all necessary documentation is completed in a timely and accurate manner.

We are seeking to appoint a hardworking and enthusiastic individual who will be able to hit the ground running. Candidates will be expected to hold a degree and have proven experience of managing research or clinical trial/project management and administration. A working knowledge of the current EU Clinical Trials Directive, UK Clinical Trials regulations, Principles of GCP, General Data Protection Regulation (GDPR) and Research Governance Framework legislation is essential. This is a fantastic opportunity for someone looking to develop their skills in project management or multi-centre RCTs within a busy research unit.

Key Responsibilities:

  • Manage the day-to-day activities of the trial, including the coordination of study staff and the management of study sites.
  • Implement trial protocols and ensure that the trial is conducted in accordance with the highest scientific and regulatory standards.
  • Ensure that all necessary documentation is completed in a timely and accurate manner.
  • Manage the associated study staff and implement / adapting established systems and processes to ensure the trial is developed and conducted to the highest scientific and regulatory standards.
  • Close liaison with the Chief Investigator and PIs at other centres.

Requirements:

  • Bachelor's degree or equivalent.
  • Previous clinical trial/project management experience.
  • Strong motivational skills.
  • Ability to work independently as well as part of a team with critical attention to detail and high levels of accuracy.
  • Effective communication, negotiation, presentation and inter-personal skills.
  • Proven excellent organisational and time management skills to effectively handle conflicting priorities and ensure tight deadlines are met.

What We Offer:

  • The opportunity to continue your career at a world-leading institution and be part of our mission to continue science for humanity.
  • Benefit from sector-leading salary and remuneration package (including 39 days off a year and generous pension schemes).
  • Get access to a range of workplace benefits including a flexible working policy from day 1, generous family leave packages, on-site leisure facilities and a cycle-to-work scheme.
  • Interest-free season ticket loan schemes for travel.
  • Be part of a diverse, inclusive, and collaborative work culture with various and resources designed to support your personal and professional development.

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