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Job Details

Clinical Research Associate

Company: Docs Global (Continental Europe)
Location: Madrid,Spain
Reference: Ref AS-025419
Closing Date: 22 Jun 18
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

This is an exciting opportunity for motivated, experienced SCRA to join one of the world´s largest providers of functional service solutions to the pharmaceutical industry and make a significant contribution to the development of new medicines that will have a real benefit for patients around the world.


Roles & Responsibilities of the position

Key responsibilities include:
Identify, select, initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with related SOP, applicable regulations and the principles of ICH –GCP and with applicable regulatory requirement.
The monitor has the responsibility to verify that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents.
To assist the Clinical Operations teams in ensuring the most effective and efficient conduct of clinical research studies.
May act as mentor for less experienced CRAs.

Job Requirements

Bachelor of Science Degree.
Preferably a Msc. in Clinical Trial Monitoring.
Min. 3 years as an independent SCRA.
Fluent in English, as well as the local language.
Excellent written and oral communication skills.
You must be available to travel.

Remuneration & other details

- Competitive salary and offer Social benefits.
- As DOCS wants to keep a good work-life balance, we offer flexible working hours and flexibility to work from home.
- HB or OB (Madrid or Barcelona).
- Long term Employment.

Apply for this job: Clinical Research Associate

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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