Pediatric Clinical Research Coordinator II

Baylor College of Medicine

Houston (TX)

On-site

USD 50,000 - 70,000

Full time

5 hours ago
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Job summary

Baylor College of Medicine in Houston is seeking a Research Coordinator to support clinical research within the USDA/ARS Children's Nutrition Research Center. The role involves coordinating research activities, maintaining regulatory documents, recruiting participants, and executing protocol procedures under the supervision of investigators.

You will work closely with physicians and study staff, ensure adherence to FDA GCP, and communicate across departments.

Qualifications

  • Bachelor's degree in a related field; four years of related experience may substitute for degree
  • One year of relevant experience required
  • Masters/MD preferred for preferred qualifications
  • Familiarity with REDCap and database maintenance is advantageous
  • Knowledge of FDA Good Clinical Practice (GCP) guidelines preferred

Responsibilities

  • Recruit research participants via phone and on-site clinics (30% effort)
  • Confirm eligibility and obtain informed consent
  • Educate participants on study procedures as needed
  • Coordinate with nursing units and schedule research visits
  • Document and maintain the research database
  • Submit research protocols for IRB and regulatory agencies
  • Perform study tasks (height/weight, questionnaires)
  • Process and ship specimens as needed
  • Prepare reports to PI, faculty, staff as required
  • Perform other duties to support the research team

Skills

Recruiting participants
IRB familiarity
FDA GCP knowledge
Data management
Communication skills

Education

Bachelor's degree
Master’s degree preferred
Medical degree preferred

Job description

Baylor College of Medicine in Houston is seeking a Research Coordinator to support clinical research within the USDA/ARS Children's Nutrition Research Center. The role involves coordinating research activities, maintaining regulatory documents, recruiting participants, and executing protocol procedures under the supervision of investigators.

You will work closely with physicians and study staff, ensure adherence to FDA GCP, and communicate across departments.

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