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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.