Clinical Trials Associate

Job type:
on-site
Start:
ASAP
Duration:
12 months
From:
Volt Europe
Place:
Middlesex
Date:
06/20/2012
Country:
flag_no United Kingdom
project ID:
380276

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Volt Life Sciences is recruiting on behalf of a leading Pharmaceutical client who are seeking a Clinical Trials Associate to work on an initial 12 month contract, supporting the team of Project Managers on Late Phase Oncology studies.

Responsibilities will include:

-Review required regulatory, financial, and legal documents from study sites for quality and accuracy.
-Track receipt of regulatory documents from study sites and submit to appropriate departments for approval of drug shipment.
-Assist in reporting and tracking of study budget spend, including processing study invoices.
-Order, assemble, distribute, manage and track inventory of study conduct tools and non-drug clinical supplies.
-Set up, obtain, and maintain sponsor regulatory, legal, and financial files per SOP.
-Assist in planning and facilitating study meetings (Investigator, CRO, Coordinator); assemble materials for study meetings; and attend meetings as needed to provide support.
-Assist in providing paper/electronic documentation to support appendices for Clinical Study Reports.

The successful candidate:

-Prior experience within a CTA type role in the Pharmaceutical or CRO sector
-Strong working knowledge of GCP and related regulatory requirements
-Exposure to Late Phase Clinical Trials is a prerequisite
-Experience of working on Oncology studies will be advantageous

Volt is an established global recruitment business with an international presence spanning the IT, digital entertainment and pharmaceutical sectors.

Volt Life Sciences recruits within biostatistics, clinical research, regulatory affairs, medical affairs, quality assurance, pharmacovigilance, market access and medical sales & marketing.