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
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