This is a flexible UK home or office based Clinical Research Associate (CRA) position with one of the leading international clinical research organisations (CRO).
You will have the opportunity to become involved in high profile projects! This company has entered a new phase of growth and as a result is looking to hire an experienced CRA at Senior CRA level to manage trial related site activities on new and ongoing phase II-IV studies.
Joining a small but dedicated and highly experienced clinical operations team you will manage all aspects of feasibility and study start up, selection, initiation, routine monitoring and close-out in the UK.
You will have core monitoring and site management responsibilities. You will manage sites in the UK but will focus on acting as a Lead CRA across Europe. You will be heavily involved in mentoring and supporting junior members of the monitoring team, attending accompanied visits and reviewing monitoring reports.
The CRA role at this company is very broad in scope and includes ethics applications, regulatory liaison, negotiating contracts with sites, managing supplies, tracking clinical budget/PI payments and helping to write clinical study reports. You will also have the opportunity to mentor and train junior CRAs
Excellent training is provided and there is plenty of scope for development into Clinical Leads and Clinical Project Managers!
Who are we looking for? You will have a proven track record of site management and monitoring in the UK across phases II-IV of development. A strong scientific or nursing background is essential for success in this role (equivalent experience will be considered).
To discuss this role in confidence, please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk
Job Ref: 8020
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