Clinical Research Associate II

Valesta is searching for an experienced CRA 2-3 years of experience so as to join our growing team of CRAs. Office-based in Madrid, the individual will work sponsor-exclusive and will be responsible for phase I (early development) trials in onco-hematology. 

Responsibilities 

While projects vary, your typical responsibilities might include: 

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution 

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. 

Profile 

Job Requirements

You should have:

  • A Bachelor's degree in a healthcare or other scientific discipline or educational equivalent
  • +2-3 years of on-site monitoring experience
  • Full proficiency of Spanish and English
  • Willingness to travel 30% 

Application form : Clinical Research Associate II

Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.
Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.

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