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Job Details

CLINICAL RESEARCH ASSOCIATE / Brussels, Belgium

Company: Covance
Location: Brussels, Belgium
Reference: 31695BR
Closing Date: 09 Feb 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. There is not better time to join us !

Requirements:


Positions : Clinical Research Associates (CRAs with 2 to 5 yrs Experience )

Locations : Belgium home-based or Brussels office-based

Given our continuous growth, we are looking for several Clinical Research Associates with:

  • A degree in life science or paramedical science
  • Clinical monitoring Experience (including pre-study, initiation, routine monitoring and close-out visits) - phase I-II-III and oncology Experience would be a plus
  • 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 langues Dutch and French
  • 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

Education/Qualifications: 

  • Degree in life science
  • 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, Dutch and French
  • Oncology Experience would be a plus
  • Good communication, planning, organization and problem solving skills

 

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: CLINICAL RESEARCH ASSOCIATE / Brussels, Belgium

Contact Information:

Address:  Covance- Brussels


Belgium
Tel: 
Fax: 
Website:  Visit Our Web Site

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