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Job Details

Experienced CRA II or SCRA in FINLAND (home based)!

Company: Covance
Location: Finland
Reference: 36689BR
Closing Date: 08 Dec 16
Type: Permanent
Salary (£): Competitive

Job Summary:

Our Clinical Research Associates manage all aspects of site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study qualification, Initiation Meetings, Routine, Interim monitoring Visits and Close-out Visits.


The CRA may serve as Lead CRA and a resource for internal and external clients. 

In order to be considered you must have the following: 

  • Life Science Degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology). 
  • Minimum of 2 years of relevant clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). 
  • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. 


  • Fluent in local office language and in English, both written and verbal 
  • In some European countries, valid drivers license 
  • Willingness to travel 
  • Must be authorized to work in the country of interest for any employer and have a minimum of 1 years relevant clinical research monitoring experience in such country 


Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

Apply for this job: Experienced CRA II or SCRA in FINLAND (home based)!

Contact Information:

Address:  Covance- Warsaw

Website:  Visit Our Web Site

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