Clinical Research Coordinator

3 weeks ago


Houston, United States Biopharma Informatic Full time

Job Description


  • Oversee overall clinical operations related to the conduct of the trial (i.e. recruitment, informed consent procedure, visit coordination, sampling, visit scheduling, etc.)
  • Skilled in reading, understanding, analyzing, and following clinical trial protocols and working strategically with study team to execute clinical trials.
  • Work in collaboration with study team to ensure trial preparation
  • Attend and participate in the Investigator Meetings (which may include travel) and any other meetings (web/telephone) as needed. Such meetings with be assigned to you by management and if they fall on the weekends, then shifts in your weekday schedule will change to accommodate.
  • Serve as main point of contacts (after SIV) for all monitoring needs.
  • Prepare for monitoring visits to make sure the monitor receives all necessary information during their visits.
  • Participate in the SQV’s, IMV’s, SIV’s and COV’s and accompany the monitor during monitoring activities.
  • IP protocols
  • Other duties and skillsets to be identified per site/per trial.
  • Follow and maintain all ethical standards as outlined in GCP training.



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