i-Pharm Consulting

Senior Clinical Research Associate

Location
England
Salary
Negotiable
Posted
14 Jan 2019
Closes
28 Jan 2019
Ref
OB1006
Contract Type
Permanent
Senior CRA – Global Pharma



i-Pharm are seeking an experienced CRA for an exciting single sponsor opportunity with a leading Pharma. They cover a wide range of therapeutic areas, including Oncology and offer an excellent training and development programme from both a leading CRO and Pharma Company.



LOCATION

UK – Home Based/ Office Based


RESPONSIBILITIES

* Working directly a leading Pharma you will implement and monitor trials across a broad spectrum of therapeutic areas
* Applying research regulatory requirements, GCP and ICH
* Present trial protocols at investigator meetings
* Liaise between study site personnel and the company



REQUIREMENTS

* Bachelor of Science or Bachelor of Nursing Degree
* 2+ years’ independent monitoring experience
* Entitlement to work in the UK
* Comprehensive presentation and communication skills.
* Oncology experience is ideal



BENEFITS

* Excellent Salary
* Car Allowance
* 25 days’ annual leave
* 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 Recruitment Consultant Olivia Baragwanath on +44 (0)20 31890469, or email obaragwanath@i-pharmconsulting.com. If this role is not suitable, Olivia is also available to discuss other possible positions or answer any general questions regarding your career and the current market.



KEY WORDS

CRA / Clinical Research Associate / SCRA / Senior Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / International Conference on Harmonisation guidelines / ICH / Oncology / Neurology/ Diabetes / Autoimmune Diseases/ Rare Diseases / England / Scotland / CRO / Contract Research Organisation / Pharmaceutical /Single Sponsor / Home Based / Outsourcing /Oncology

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