Achieva Group Ltd

CRAII/SCRA

Location
Midlands
Salary
Not specified
Posted
09 Feb 2021
Closes
11 Mar 2021
Ref
BH-6000
Contact
Lewis Coulson
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
We are looking in our FSP team for ideally Sr CRA or CRA II for the UK. Same requirements as normal but just working for one single sponsor and be happy to work with a large Pharma only.
 
We want them to be based in the Midlands or North due to COVID travel restrictions so it will be to cover the sites we have in those areas. The team will not consider people in London / South/ South West / South East at the moment.
 
Please remember on the JD they will only do the CRA tasks so “Maintenance from initiation through close out “parts.  These tasks are all done by the CRA.

Personality :  Proactive – strong communicator – good time management – good attention to detail  - resilient & be able to push back – personable – flexible – professional – confident– can work under pressure – can work as part of a team – collaborative – accountable – client / customer focused  

Qualifications
:

Need a degree in Life Science, Nursing or Pharmacy (essential – they must have a related Life Science degree as a minimum)

·         Working as part of the UK Clinical Operations FSP group of approx. 10 people in the UK.
·         They will be national monitoring for 4-5 studies at approximately 10 sites in total.
·         The uncertainty of the COVID situation means that we require CRAs who live closer to the sites that we are managing.
·         So, a CRA is required in Midlands to help us with sites all over the middle of England.  Once COVID restrictions are lifted, we can look at more national coverage if required, such as London sites.
·         They would report to a Clinical Operations Manager
·         Previous CRO or Pharma industry experience within clinical operations is essential.
·         Must have strong previous clinical onsite monitoring experience as a CRA.
·         Dealing with multiple projects (studies / protocols) is important but for 1 sponsor.
·         Strong ICH - GCP knowledge is essential
·         Good UK Regulatory knowledge / understanding of MHRA is required   
·         Any Therapeutic Area experience is ok but a strong preference for Oncology / Respiratory
·         Approx. 2-3yrs+  monitoring experience as a CRA for the CRA II level
·         Approx. 3-5 year yrs + monitoring experience  for the Sr CRA level.
·         UK based monitoring experience is essential
·         Client facing experience is very important and customer service skills as will be managing the site / points of contact
 
·         Location:  Midlands or North  England based
·         Must hold a Full UK license / European Driving license and be willing to drive.
·         They must be willing to travel  1.5 – 2 per week, over time it will be to any UK location or region but for the time being it will be the North / Midlands sites.
·         They must be happy with doing approx. 6-8 onsite monitoring activity days per  month
 

Apply for CRAII/SCRA

Already uploaded your CV? Sign in to apply instantly

Apply

Upload from your computer

Or import from cloud storage

Your CV must be a .doc, .pdf, .docx, .rtf, and no bigger than 1MB


4000 characters left

Marketing Communication

We'd love to send you information about Jobs and Services from PharmiWeb.jobs by email.

All emails will contain a link in the footer to enable you to unsubscribe at any time.


When you apply for a job we will send your application to the named recruiter, who may contact you. By applying for a job listed on PharmiWeb.jobs you agree to our terms and conditions and privacy policy. You should never be required to provide bank account details. If you are, please email us.

Similar jobs

Similar jobs