Principal CRA

Middlesex  ‐ Onsite
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Keywords

Description

This person be responsible for duties including:
-Managing the European component of global PII-III outsourced studies
-Supervising and coordinating all aspects of the clinical studies
-Conducting co-monitoring as required
-Drafting and coordinating review of relevant documents such as protocols, informed consents, case report forms, monitoring plans, etc.
-Contributing to the development of study budgets
-Maintaining study timelines
-Contributing to the development of RFPs and participating in the selection of CROs/vendors as well as managing them
-Coordinating review of data listings and preparing clinical study reports
-Travelling internationally 20% of the time

Essential Qualifications:
-A minimum of 4 years of experience performing related duties
-UK/European experience mandatory
-Previous Pharmaceutical experience in Europe ideal
-Experience in study management/coordination of multinational EU clinical trials
-Monitoring experience
-In depth knowledge of FDA and EMEA regulations, ICH guidelines, and GCPs

Candidate should send CVs or contact Andrew directly.

Allegis Group Limited and Aston Carter Limited operate Employment Businesses and Agencies and are companies within the Allegis Group Inc. group of companies, the fourth largest staffing company in the world, (collectively referred to as the "Allegis Group"). TEKsystems and Aerotek are divisions of Allegis Group Limited. Applicant data will be treated in accordance with the Allegis Group's Privacy Notice.

Start date
01/11/2012
Duration
12 months
From
Aerotek
Published at
04.10.2012
Project ID:
429283
Contract type
Freelance
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