Clinical Research Associate

4 days ago


Sacramento, California, United States Medix™ Full time
Clinical Research Coordinator

We are seeking a highly skilled Clinical Research Coordinator to support our team in managing and coordinating clinical trials and research studies. The ideal candidate will have a strong understanding of regulatory guidelines and protocols, as well as excellent communication and organizational skills.

Key Responsibilities:
  • Coordinate and oversee all aspects of clinical trials, including participant recruitment, enrollment, and follow-up.
  • Assist in the development of study protocols, consent forms, and data collection tools.
  • Ensure all research activities comply with ethical standards, institutional policies, and regulatory requirements.
  • Collect, manage, and analyze clinical data; maintain accurate and organized records.
  • Communicate with study sponsors, monitor study progress, and resolve any issues that arise.
  • Schedule and conduct participant visits, ensuring compliance with study protocols.
  • Assist with the preparation of regulatory documents and reports.
  • Maintain confidentiality and protect the integrity of participant data.

Requirements:

  • Strong understanding of clinical research principles and regulatory guidelines.
  • Excellent communication and organizational skills.
  • Ability to work independently and as part of a team.
  • Strong attention to detail and ability to maintain accurate records.


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