i-Pharm Consulting

CRA / SCRA – Regional Monitoring – UK

Location
South West England
Salary
Negotiable
Posted
20 Nov 2018
Closes
05 Feb 2019
Ref
CNOB665
Contract Type
Permanent
Seeking a hardworking and driven CRA with 1.5+ years’ UK monitoring experience. My client is a leading CRO that is searching for a CRA to join their team and cover sites in the South West of England. This role offers you a great work-life balance with a low protocol load and regional monitoring.

LOCATION

UK – Regional Monitoring

REQUIREMENTS

* Bachelor of Science or Bachelor of Nursing Degree
* 1.5+ years monitoring experience
* Entitlement to work in the UK
* Full UK drivers licence



BENEFITS

* Excellent Salary
* Car allowance or Car
* Healthcare
* 25 days’ annual leave
* Pension



RESPONSIBILITIES

* Conduct site initiation visits, routine monitoring visits, and close-out visits
* Liaise with the PI and site staff
* Apply research regulatory requirements, GCP and ICH.
* Present findings at investigator meetings and to discuss budgets with potential investigators





ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.



www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Recruitment Consultant Ciara Noble on +44 (0)20 31890469, or email cnoble@i-pharmconsulting.com. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.



KEY WORDS

CRA / CRA II / Clinical Research Associate / SCRA / Senior Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / CNS / England / South West England / Major Pharma’s / Sponsor Pharma’s / CRO / Contract Research Organisation / Pharmaceutical /Multiple Sponsors / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits /

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