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Job Details

Clinical Research Associate (CRA) - Netherlands

Company: Covance
Location: Netherlands
Reference: 67809BR
Closing Date: 03 May 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Covance is one of the world's most exciting and professional drug development services companies (CRO), providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.

Requirements:

Position : Clinical Research Associates (CRA)

Location : The Netherlands – home-based or (partly) client office-based

Divisions : Outsourcing, Clinical Operations, Early Clinical Development

Due to our constantly growing business needs we are looking for Clinical Research Associates with:

  • A minimum of 2 up to 5 years clinical monitoring Experience (including pre-study, initiation, routine monitoring and close-out visits) - oncology Experience would be a plus
  • University/college degree (life science preferred), or certification in a related allied health profession (e.g. nursing certification, medical or laboratory technology).
  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
  • A full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Fluency in English and local language
  • Good communication, planning, organization and problem solving skills

Education:

  • University/college degree (life science preferred), or certification in a related allied health profession (e.g. nursing certification, medical or laboratory technology).

Experience:

  • Two up to four years of clinical monitoring Experience (including pre-study, initiation, routine monitoring and close-out visits)
  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
  • Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Fluency in English and local language
  • Oncology Experience would be a plus
  • Good communication, planning, organization and problem solving skills


Your rewards:

  • The opportunity to pursue further training and an interesting career in an inspiring environment that values achievement, supports a balance between your personal and professional life and allows you to make meaningful contributions
  • Flexible conditions and an attractive remuneration package

 

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.

 

Keywords: Clinical Research, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA,  Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical

Apply for this job: Clinical Research Associate (CRA) - Netherlands

Contact Information:

Address:  Covance- Warsaw


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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