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What you will do:

  • Responsible for managing the research activities at sites.
  • Involved in identifying potential sites and performing study start-up activities.
  • Required to ensure compliance with obtaining informed consent.

What you will bring to the role:

  • Excellent interpersonal, oral, and written communication skills in English.
  • Superior organizational skills with attention to details.
  • Ability to work with little or no supervision.

Your experience:

  • 5+ years of experience as a Clinical Research Associate.
  • 4-year university degree or RN/BSN in Nursing.
  • Willingness to travel required.

Worldwide Clinical Trials

Worldwide Clinical Trials is a global, midsize CRO that pushes boundaries, innovates and invents to cure the world’s most persistent diseases. They are a global team of over 3,500+ experts, bright thinkers, dreamers and doers that are changing the way the world experiences CROs.

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