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Clinical Research Associate Job Description

We are looking for an proactive and ambitious Clinical Research Associate to join our growing company. The ideal individual will be passionate about making charts, collecting data, and working at the cutting-edge of scientific breakthroughs. Your responsibilities will include coordinating clinical research projects. You will oversee the research team and ensure objectives are met, and the proper protocols are followed.

Clinical Research Associate Responsibilities

  • Direct and plan clinical research projects and trials
  • Supervise employees undertaking clinical research
  • Provide team training and highlight professional development opportunities
  • Recruit study participants, and obtain and document participant’s informed consent
  • Monitor the ongoing research to maintain compliance with government regulations and scientific protocols
  • Collaborate with ethics committees, ensuring research activities adhere to the highest standards
  • Design protocols for clinical research trials
  • Screen potential trial participants through interviews, medical records reviews, and follow-ups with nurses and doctors
  • Maintain accurate records of research activity, including case reports, informed regulatory forms, consent forms, and drug dispensation records
  • Verify data, compile findings, and present results
  • Seek out opportunities for continued education

Clinical Research Associate Requirements

  • Clinical Research Coordinator
  • Clinical Research Administrator
  • Clinical Programme Coordinator
  • Clinical Programme Manager
  • Strong oral and written communication skills
  • Detail-oriented and able to perform complex tasks with a high level of accuracy
  • Excellent deductive reasoning, decision-making, and problem-solving skills
  • Excellent time management
  • Able to prioritise tasks and achieve set goals efficiently

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