Research Study Manager

2 weeks ago


San Marcos, Texas, United States Medix™ Full time

Medix™ is looking for a meticulous Clinical Trials Coordinator to enhance our research team. In this position, you will oversee and facilitate clinical trials, ensuring adherence to study protocols and maintaining comprehensive documentation. You will collaborate with researchers, participants, and sponsors to support various study operations, including participant recruitment, data management, and reporting. The ideal candidate will possess strong organizational abilities, a background in clinical research, and a solid grasp of regulatory standards.

Primary Responsibilities:

  • Oversee and coordinate the daily operations of clinical trials.
  • Identify, screen, and enroll participants in accordance with study protocols.
  • Secure informed consent and prioritize the rights and safety of participants.
  • Collect, process, and manage clinical data and biological samples.
  • Maintain precise and thorough records of all study-related activities.
  • Monitor participant progress and document any adverse events.
  • Ensure compliance with Good Clinical Practice (GCP) and relevant regulatory guidelines.
  • Prepare and submit necessary documentation to Institutional Review Boards (IRBs).
  • Assist in the formulation and modification of study protocols and procedures.
  • Work collaboratively with researchers, sponsors, and regulatory entities to ensure efficient study execution.


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