Clinical Research Associate

Location
Bolton, Greater Manchester (GB)
Salary
Excellent benefits package including Salary & Car Allowance
Posted
11 Jan 2021
Closes
10 Feb 2021
Ref
AG072
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Clinical Research Associate

Office based in Greater Manchester

My client, a smaller global organisation with a European presence are looking for an experienced CRA to join their business as a CRA with additional responsibilities.

If you are looking for an opportunity to broaden your career, work on some truly fascinating studies in very niche therapeutic areas, or even just a genuine chance of ongoing career development then I am confident this could be the perfect organisation for you.  The beauty of this client is that they focus on multiple therapy areas across all phases of the clinical trial spectrum which means no matter what your previous exposure has been there could be a perfect opportunity waiting for you.

New medicine development is at the forefront of everyone’s mind at the moment and this is a truly innovative business who are constantly looking for ways to change and better the future of the life sciences industry and are an admired company to work for this year because of this.

If this isn’t enough to make you want to apply then its also worth mentioning that this is a company who also take their corporate social responsibilities seriously, whether that be ways to prevent pollution and carbon emissions or more simply supporting causes that are important to their employees this is at the core of what they do.

As a CRA your responsibilities will include:

·        Coordinating Phase I-IV clinical trials

·        Performing the full range of site visits: qualification, initiation, monitoring, motivational, audit support, and close out.

·        Identifying and conducting feasibility assessments for proposed study sites in conjunction with the Project Team.

·        Liaising with other appropriate departments to ensure the smooth running of the study

·        Involved in submissions for Ethics and Regulations on new studies

Your previous experience should include:

A degree in life science or related and experience of independent monitoring within clinical research, including good clinical knowledge with an understanding of medical terminology.

In addition, previous experience of the Clinical Trials industry in a Study Coordinator or Clinical Trials Associate role would be an advantage.

This position is office based in the UK and therefore flexibility to travel will be essential.

To know more about this terrific company and to get a better feel for whether this position falls in line with your expectations, please speak to Alex Goodman by applying with your CV or contacting directly using the below contact information:

+44 (0)1293 584 30

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