SCRA - Senior Clinical Research Associate - Field based UK

Recruiter
RBW Consulting Solutions Ltd
Location
Manchester
Posted
10 Feb 2018
Closes
15 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
I am recruiting for several SCRAs / Senior Clinical Research Associates - for one of my clients, a leading, global drug development organisation, as they expand their clinical operations team to welcome an experienced Senior Clinical Research Associate (SCRA) to work on a key study at sites within the UK. This position can be office based in the South, South East or Scotland offices, or in a remote, home-based position.

This is a good opportunity for an experienced CRA to work with a global CRO with a top reputation. Our client can provide opportunities to work an interesting variety of therapeutic areas (such as rare diseases and CNS / Neurosciences and Endochrinology) from a range of sponsors giving you exposure to a mix of interesting projects.

These form part of global projects and will vary from Early phase to Late Phase / Observational studies

Our client has a low staff turnover and works hard to maintain a good Life / Work balanceand you will be supported by an excellent clinical manager.

Our client will also be help you achieve your longer term career aims; whether you wish to develop your career towards Clinical Project Management, Regulatory Affairs or Clinical Operations / CRA Manager.

This opportunity will suit a CRA who is perhaps keen to settle with an established, successful CRO with a strong pipeline of studies and excellent, global clinical development functions.

The ideal professional will be an enthusiastic CRA with positive communication skills and have excellent relationship-building abilities whilst working in a collaborative way with site staff such as Clinical Research Nurses, Study Site coordinators and Principle Investigators.

As a SCRA, you will may also provide study training where required for more junior CRAs. You should also be detail orientated where you will evaluate the quality of site data and escalate any quality issues to the relevant team manager.

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

You should be educated to degree level in life sciences and have a full UK driving licence.

To learn more about this position and to discuss your career development requirements, get in touch with me, Simon Penrose, via the contact details aside.

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