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Study Coordinator

A great opportunity for an experienced Trial Coordinator who loves to share his/her experience and knowledge.

Job Description

Within this project, you will support a study coordinator with the preparation and follow up of two clinical trials focussed on Multiple Sclerosis. You will help create worksheets, prepare the on-site visits of trial participants and are responsible for the data entry.

Responsibilities

  • Support the local site personnel with two Multiple Sclerosis clinical trials
  • Data entry and data management
  • Contact with site personnel
  • Preparation of patient visits
  • Planning of Trial visits
  • Contact with the Sponsor

Requirements

  • A degree in life sciences
  • 1 to 5 years of experience in coordinating clinical trials
  • Good knowledge of ICH-GCP
  • Experience in Multiple Sclerosis is a plus but not a must
  • Affinity for electronic devices (Tablets, electronic questionnaires, smartwatches, etc.)
  • Very strong time management skills
  • Languages: French, English
  • Strong communication skills
  • Team player
  • Flexibility
  • Strong organizational skills
  • Stress resistant

Benefits

  • Salary based on your capabilities and experience
  • Freelance position for 1 day a month, for approx. 2 years

Existing right to work in Europe required ( please read job spec in full before applying ).

Vacancy number: 17623