Vitalograph UK Vacancies

Role: Associate Project Manager

The role has the following key responsibilities:
  • Assisting Project Manager / Senior Project Manager with general study duties.
  • Assisting with and taking ownership of Project management tasks and day to day running of clinical trials projects involving centralized systems as requested by the Program Manager, Senior Project Manager / Project Manager.
  • Project Managing assigned Clinical Trials and internal projects.
  • Ensuring GCP compliance.
  • Assisting with the specification, setup and despatch of non-centralized systems where customised software is to be used.
  • Chairing and documenting project meetings.
  • Reporting on study progress.
  • Problem solving project issues.
  • Training Monitors and Investigators (at Investigator meetings, on site, or providing additional training via the telephone/web).
  • Writing and updating relevant SOPs.
  • Writing study related documents as requested by Project Team.
  • Assisting with writing, updating and printing study manuals.
  • Ensuring any study related documents are filed and stored appropriately.
  • Management of Project Coordinators (as advised)
  • Gathering information on Pharmaceutical and Biotech companies (as required) to assist other members of Vitalograph team with sales opportunities.
  • Involvement in bid-defence meetings.
  • Attending conferences in a sales capacity for Vitalograph.
Outline of skills required:
  • Organisational skills and the ability to use project management tools
  • Understanding of GCP
  • Ability to demonstrate / train on Vitalograph products and systems
  • Communication and Presentation skills
Experience Required:
  • Previous experience of project management (not necessarily in a PM role).
  • Desirable: experience in a clinical trials environment (Sponsor/CRO/Site).

If you are interested in the above position, please apply using the link below, including a brief cover letter and a detailed CV.