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gcp monitoring clinical research ich crm tools
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πŸ“‹ Description

  • Serve as a main point of contact for investigative sites
  • Build and maintain strong working relationships with site staff and investigators
  • Conduct site engagement calls and regular site contact
  • Support site monitoring activities to ensure protocol compliance and quality conduct of the trial
  • Participate in site evaluation, site training, routine monitoring, and site closure activities
  • Help sites understand the study protocol, treatment principles, and operational expectations

🎯 Requirements

  • Degree in pharmacy, biomedicine, nursing, medicine, or another science-related discipline
  • Knowledge of therapeutic areas and ability to apply scientific concepts to clinical trial conduct
  • Strong planning, organisational, and time-management skills
  • Ability to work effectively in a dynamic environment with competing priorities and deadlines
  • Strong interpersonal skills - written, verbal, and listening skills
  • Comfortable using systems, tools, and technology to support site needs

🎁 Benefits

  • Hybrid office-based position
  • Career development in clinical research
  • Work in a collaborative Nordic team
  • Direct involvement in clinical research operations
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