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SCRA – Senior Clinical Research Associate in South East, England

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Location
South East, England
Salary
Negotiable
Job type
Permanent
Category
Clinical/Medical, Project Manager
Job Id
SP/SCOB/6
Posted on
31 Mar 2017
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About the Role:

A leading drug development organisation

One of my clients, a leading drug development organisation, is expanding their team to welcome an experienced Senior Clinical Research Associate (SCRA) to work regionally across Southern England. This position can be office based in the South East or in a remote, homebased position.

This is to take responsibility and oversight of several sights based along the South coast and within the M4 corridor / Bucks & Berks region.

This is a good opportunity to work with a global CRO who are able to work with you to help you achieve your longer term career aims; whether you wish to develop your career towards Clinical Project Management, Regulatory Affairs or Clinical Operations.

Although not aligned to one specific therapeutic area, the initial work will see you involved in Cardiovascular projects where you can make a key contribution to a critical study. These form part of global projects and will vary from Early phase to Late Phase studies.

The ideal professional will have excellent relationship-building skills and will enjoy working in a collaborative way with site staff such as Clinical Research Nurses, Study Site coordinators and Principle Investigators and also provide study training where required. You should also be detail orientated where you will evaluate the quality of site activity and escalate any quality issues to the relevant team manager.

It is also essential that you can work affectively with a range of colleagues from within clinical operations such as members of the Clinical Project Management team, Regulatory Affairs & Clinical Data Management.

You will be given the opportunity to support several different project at various stages in their lifecycle. Therefore, you will be required to support projects ranging from site selection and initiation, through to site monitoring and study close-out visits, tracking any regulatory submissions, supporting patient recruitment procedures and looking to resolve any data queries.

You should be educated to degree level in life sciences or equivalent subject and have approx. 2-3 years CRA experience and have a full UK driving licence.

Salary: On application

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