Senior Clinical Research Associate - Italy
- Employer
- RBW Consulting
- Location
- Milan, Italy
- Salary
- Attractive package including competitive salary, car allowance, annual bonus & daily meal allowance
- Start date
- 14 Jan 2021
- Closing date
- 13 Feb 2021
View more
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Senior Clinical Research Associate
Italy – Office Based in Milan
My client, a Mid-Size global organisation with a large European presence are looking for an experienced CRA to join their business as a Senior CRA.
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 mind, this is a truly innovative business who are constantly looking for ways to change and better the future of the life sciences industry and as a result have been listed as one of the most admired companies to work for this year.
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
· Partner with Regulatory Specialists to undertake submissions as a local level
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.
Previous working experience of Clinical Trial submissions at a local level in Italy
In addition, previous experience in mentoring and coaching CRAs would be highly advantageous.
This position is based at the company’s offices in Milan and therefore flexibility to travel from Milan across Italy will be essential.
You must also be able to speak both Italian and English fluently and have the right to work in Italy.
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 584 300
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