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Partnerships in Clinical Trials 2014

Reference No: J11424

Clinical Research Associate - CRA II

Are you looking for an exciting opportunity and have a passion for Clinical Research? An excellent opportunity has arisen with a leading, Global CRO.

Location: Madrid
Salary guide: €34,000 – €36,000
Duration: Permanent, full time

Core Responsibilities:

•Site administration and monitoring (initiation, maintenance and close-out)
•Working to ICH guidelines and GCP.
•Recruiting potential investigators, preparing submissions, vendor management
•Completing Serious Adverse Event (SAE) reporting
•Trial Master File set-up and maintenance: in-house and Investigator site files
•Negotiating and tracking study budgets and contracts
•Writing SOP’s

Qualifications/experience required:

•1.5 years + CRO and monitoring experience either working in a CRO or Pharmaceutical company
•Life science degree or equivalent
•Good understanding of the clinical trial process
•Excellent written and oral communication
•Able to travel around Spain for site visits, approximately 60-70% travelling
•Fluent English skills & Spanish

If you are interested please contact:
Josh Larwood on +44 (0) 0207 822 1710 or josh.larwood@clinicalprofessionals.eu

If however, you do not feel that this is the right role for you, please forward these details on as we have a generous referral scheme in place.

Please note due to the high level of applications if you are not contacted within 48 hour, you have not been successful on this occasion.
Key Words: CRA II, Monitoring, CRO, Pharmaceutical, Life Sciences, ICH, SOP’s, Spain, Madrid

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