CRA II / Senior CRA - Global CRO - UK

This leading international CRO is seeking a CRA II/Senior CRA to join their team in the UK. This is an excellent opportunity to work with leading sponsor clients on a range of therapy areas including Oncology. This is a great opportunity for CRAs with 1+ years' independent monitoring experience to work with a global pharma sponsor that is well recognised in the industry and has a proven route of progression.

LOCATION

UK - Home or Office based

ROLE/DESCRIPTION

You will have 1+ years CRA experience including site selection, routine monitoring and close-out visits. You will have knowledge of and skill in applying clinical research regulatory requirements, GCP and ICH.

This position requires you to perform all clinical site management and monitoring activities including the conduction of qualification visits, site initiation visits and monitoring visits. You will act as the direct contact for assigned clinical sites and will carry out all necessary site documentation verification. You will be required to act as a mentor to other CRA members and to assist them in their training and development.

COMPANY

This globally known and well renowned CRO works on a broad portfolio of trials with a particular focus on Oncology. They focus on world class training and limited protocol load which ensures greater job satisfaction. The company has a network of 40,000+ employees and operates in over 50 countries.

REQUIREMENTS

• Bachelor of Science or Bachelor of Nursing Degree
• 1+ years independent monitoring experience
• Thorough knowledge of GCP and ICH
• Strong working knowledge of EDC systems and IVRS is desirable
• Competent in written and oral English
• Entitlement to work in the UK
• Full drivers' licence

BENEFITS

• Excellent Salary
• Company car or car allowance
• Healthcare
• Life Assurance
• 25 days' annual leave
• Pension
• Flexi Benefits

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 Business Manager Ciara Noble on +44 203 189 0469, 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 / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / England / South England / London / South West / South East / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Global Pharma /