Clinical Research Associate II

We are currently looking to strengthen our Clinical Monitoring team in Spain and are seeking a Clinical Research Associate II for onco-hematology phase I trials. CRA will be exclusively sponsor-based in Madrid with a permanent contract.  

 

 

Responsibilities 

International Clinical Trials onco-hematology phase I.

Monitor the conduct of clinical trials, especially enrolment and quality of data.
Verify subject safety and site adherence to ICH/GCP Guidelines.
Ensure Adverse Events are reported appropriately, accurately and in a timely manner and that follow-up activities are conducted as necessary.
Review e-CRF, Informed Consent Documents and query language/narratives.
Acquire specific clinical and therapeutic knowledge related to studies monitored.
Conduct Qualification, Initiation, Interim and Close out monitoring visits.
Ensure complete and thorough study Investigational Product reconciliation.
Manage trip reports, letters, query resolutions and expenses.
Manage site master file contents and work with sites to ensure communication requirements between site and IRB are adhered to.
Investigator meetings management.

Profile 

Life Sciences Degree 

Previous experience as a CRA minimum 2 years in SIV, MV and SCV. Desirable sponsor-based but not limited. 

English is a must (C1) 

Able to travel up to 40% Spain. 

 

Contact Information 

If you feel interested in this opportunity please send your CV and enclosed application letter to recruitSpain@valesta.com

Our team of recruiters will review your CV and if your experience matches to the opportunity they will contact you. 

Many thanks!

Application form : Clinical Research Associate II

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