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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
Benefits:

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.

Requirements:

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 


THERE IS NO BETTER TIME TO JOIN US!

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


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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