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Job Details

CTA Belgium

Company: Chiltern
Location: Ghent, Belgium
Reference: IdH898972
Closing Date: 01 Jan 17
Type: Full Time
Salary (£): On Application

Job Summary:

The role is to do the administration for international Phase I/II trials.


We are looking for a Clinical Trial Associate to work for our client a small Biotech company located in Belgium. This organization develops drugs based on human antibodies for orphan / rare diseases (oncology and immunology).

Duties & Responsibilities

  • Be accountable for providing logistical support for a clinical program and associated clinical trials
  • Be accountable for delivery of complete Trial Master File (TMF) for assigned studies or program
  • Be responsible for the collection, review and tracking of regulatory documents for assigned clinical studies
  • Be responsible for the timely and accurate input of study-related information into Impact
  • Be responsible for preparation and distribution of regulatory and operational binders/manuals and clinical system set-up
  • Be responsible for processing clinical grant payments to investigative sites and clinical trial material requests
  • Provide oversight and quality assessment of document standards, tools and processes at the program level
  • Act as a primary logistical point of contact with investigative sites



  • BA/BS/BSN degree is required
  • At least 3 years previous experience in the healthcare field; pharma experience strongly preferred; with a basic understanding of drug development and knowledge of ICH and GCP guidelines is desired
  • Must have good interpersonal, written and verbal communication skills and strong computer skills
  • Fluent in English
  • Should be a team player capable of working in a multi-cultural environment
  • Only candidates living in Belgium are invited to apply.

Apply for this job: CTA Belgium

Contact Information:

Address:  Netherlands
Schipholweg 111, 2316 XC Leiden, Netherlands

Tel:  +31 71 711 2500
Website:  Visit Our Web Site

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