AP-PM-3185: Clinical Research Project Manager - Cardiac Monitoring
  • Consultant:
    Stephen Pimm
  • Published:
    20 May 2019
  • Location:
    United Kingdom - UK + travel to Reading, Stockport, Bristol and Newcastle
  • Sector:
    Health and social care
  • Type:
    Contract
  • Offering:
    To £300 per day - for an initial 3 month full time followed by 9 months at part time (2-3 days)
  • Start Date:
    ASAP - Post Interviews
Job Description:

A contract project manager is required for a 12-month (3-month full time/9-month part time) role to deliver a clinical research - cardiac monitoring project.

 

 

Our client is a manufacturer of a cardiac monitoring solution that is currently being tested in a major UK based clinical research trial. This project has the potential to run between 1-3 years, engage up to 30K people and will take place over four locations: Newcastle, Stockport, Bristol and Reading. Travel between all sites is required.

You will act as the client representative, engaging multiple partner organisations based across the US, UK and Europe. Full time for the first 3-months with part time working for the remaining 9-months

 

Key tasks:

  • Manage the project in the UK and work with all key parties (Client, Data Analysis Partner, Logistics Partners) to ensure the successful delivery of our client’s clinical services
  • Develop detailed project plans for study launch and ongoing management and work with all parties to track and manage to plan
  • Participate in and run weekly project management meetings with all involved parties
  • Serve as the primary point of contact for the Client centres for support and logistical questions
  • Assist in design and implementation of all processes and systems (logistics, dataflows, IT) required to support the client project
  • Manage the “go-live” process for each imaging site, including providing onsite training to Client staff
  • Monitor KPIs for the project and provide regular reporting to client management

 

Essential experience:

  • Demonstrable full lifecycle project management experience within a healthcare environment.
  • Prior clinical study management experience across all stages of the study project, including planning/startup, execution, and closure, preferably in medical device.
  • Excellent client facing experience – must have strong stakeholder management skills and experience.
  • Degree educated (ideally Masters) or equivalent experience – in a scientific discipline.
  • Ability to make high level decisions and work collaboratively and effectively within a team.
  • Strong verbal communication and writing skills.
  • Working knowledge of scientific and statistical principles and analysis/presentation/ reporting of data collected in clinical trials.
  • High degree of computer proficiency and understanding of IT systems
  • Highly detail-oriented.
  • Demonstrated track record of driving projects/deliverables to completion with established deadlines.
  • Excellent time management and organizational skills.
  • Ability to work collaboratively and effectively with people remotely and across different time zones

 

 

Our client requires this resource URGENTLY – only candidate who are immediately available will be considered.

Skills:
Not Specified
Person Specification:
Not Specified

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