Senior CRA/Associate Project Manager

Senior Clinical Research Associate/Associate Clinical Project Manager

Home Based anywhere across Spain.

My client, a small global organisation with a growing presence in Europe and I am helping them to identify a Senior CRA to join their business and work with them across different studies and manage those studies in Spain alongside the European Project Managers based in the UK.

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 everything they do, even to the point where all profits that are made by the full service CRO business are used to support the wider foundations Cancer research network. Meaning that not only are the companies staff supporting the development of new treatments for patients, but they are also contributing towards the advancement of potentially life saving cancer treatments by simply doing their jobs.

If this is not enough to make you want to apply then its also worth mentioning that this company 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 across Spain

·        Working alongside European Project Managers (remotely) and supporting the progress of important trials by working with Spanish sites on elements such as patient recruitment

·        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 studies.

·        Future management responsibilities as the team in Spain grow and more professionals join the company

Your previous experience should include:

A degree in life science or related and experience of independent monitoring within clinical research, including good clinical knowledge and working understanding of GCP Regulations.

In addition, previous experience within any other Clinical function would be highly advantageous. It is also expected that you will have worked for a Clinical Research Organisation previously during your career.

This position is home based anywhere across Spain 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 using the below contact information:

+44 (0)1293 584 30