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Clinical Research Associate

2 months ago

Nottingham, Nottingham, United Kingdom Actalent Full time
Job Opportunity

This is an exciting opportunity to work with a dynamic team in a clinical research setting.

The Study Coordinator will be responsible for managing day-to-day activities, including reporting adverse events, data entry, and administrative tasks. They will also be involved in query resolution and work closely with the team to ensure the success of the study.

Oncology and Hematology experience is highly valued in this role, but not required.

Key Responsibilities:

  • Manage study-related activities, including data entry and query resolution
  • Report adverse events and ensure timely follow-up
  • Collaborate with the team to achieve study goals
  • Perform administrative tasks, including document management and filing

Requirements:

  • Minimum 1 year of clinical research experience
  • Ability to work independently and as part of a team
  • Strong organizational and communication skills