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Joboffer number #236969

Clinical Research Associates all levels

CV Market client
Lithuania
Nuoroda nukopijuota
Job ad expired!

Job Description

  • Site administrating and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP;
  • Recruiting potential investigators, working with start-up department for EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
  • Completing Serious Adverse Event (SAE) reporting, processing production of reports;
  • Negotiating study budgets with potential investigators and assisting the Covance legal department with statements of agreements as assigned.


Requirements

About You:

  • University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology);
  • Fluency in local and English language.
  • Understanding of the clinical trial process;
  • Minimum 1 year of monitoring experience in pharmaceutical or CRO industries;
  • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements;
  • Thorough knowledge of monitoring procedures.


Company offers

How to apply:

To apply, please visit our website at careers.covance.com and look for the reference 44909BR.

You can also follow the link: http://careers.covance.com/job-postings/44909BR/clinical-research-associates-1-or-2-or-senior



EEO Employer: 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.


Darbo skelbimo numeris
#236969
Jūs kandidatuojate į:
Clinical Research Associates all levels
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