i-Pharm Consulting

Clinical Research Associte

Location
England
Salary
Negotiable
Posted
10 Jan 2019
Closes
24 Jan 2019
Ref
OB1004
Contract Type
Permanent
CRAII/Senior CRA - Cardiology

This mid-sized award winning CRO are seeking an experienced CRA II/Senior CRA with experience working on Cardiovascular studies. This is an excellent opportunity for CRA with 2 + years’ experience to join a Global CRO that offers clear career progression opportunities.

LOCATION

UK – Home Based


RESPONSIBILITIES

* Working directly a leading CRO you will implement and monitor trials across a broad spectrum of therapeutic areas including Oncology
* 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
* Experience working within Cardiovascular studies
* Entitlement to work in the UK
* Comprehensive presentation and communication skills.



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

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