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Study Coordinator

  • Location:

    Woluwe-Saint-Lambert

  • Contact:

    Charlotte Evens

  • Job type:

    Contract

  • Contact phone:

    +32 15 28 40 43

  • Industry:

    Life Sciences, Clinical Research

  • Contact email:

    charlotte_evens@oxfordcorp.com

If you are looking for a challenging Study coordinator position within an oncologic Phase 1 unit then this is the place to be.

Job Description

You will be responsible for the coordination of clinical trials from A to Z in a very dynamic team.

Responsibilities

  • Coordination of Phase I oncology clinical trials
  • Data entry and data management
  • Contact with patients
  • Data collection during patient visits
  • Planning of Trial visits
  • Safety reporting (AE, SAE's)
  • Administrative follow up (e.g. Investigator Site File)
  • IMP handling

Requirements

  • A degree in life sciences
  • 1 to 5 years of experience in coordinating clinical trials
  • Good knowledge of oncology
  • Good knowledge of ICH-GCP
  • Experience in early phases trials is a plus
  • Very strong time management skills
  • Languages: French, English
  • Strong communication skills
  • Autodidact
  • Proactivity
  • Team player
  • Flexibility
  • Strong organizational skills
  • Stress resistant

Benefits

  • Full time or part time position
  • A balanced salary package based on your capabilities and experience

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

Vacancy number: 17207