Clinical Research Coordinator

1 week ago


Chesterfield Missouri, United States Headlands Research Full time

Job Summary:

Clinical Research Professionals, a dedicated research center, is seeking a highly skilled Clinical Research Coordinator to manage clinical research protocols. As a key member of our team, you will work closely with investigators and research staff to ensure protocol visits are conducted according to ICH GCP guidelines.

Responsibilities:

  • Comprehend study design of each protocol assigned
  • Obtain informed consent from study participants
  • Perform procedures in compliance with the study protocol
  • Screen study subjects according to specific protocol requirements
  • Collect and record study data in source documents via electronic system (CRIO)
  • Manage study-related activities
  • Ensure adherence to protocol requirements
  • Review laboratory data
  • Assess and document compliance
  • Manage investigational product
  • Assess, record, and report Adverse Events as outlined in the protocol
  • Manage/train ancillary staff

Qualifications:

  • Experience and training in conducting clinical trials with knowledge of ICH GCP
  • Licensed Nurse in Missouri - RN or LVN/LPN (Strongly Preferred)
  • IV Certification, if LPN
  • Degree in a health or scientific related program strongly preferred
  • Excellent interpersonal and communication skills: Able to interact effectively with professional and administrative staff, sponsor and regulatory representatives
  • Compassion for patients (study participants)
  • Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing lab specimens
  • Excellent written & oral communication skills
  • Have a passion for clinical research and helping people
  • Experience with CRIO (Clinical Trial Management System) is a plus
  • Experience with administering vaccines is a plus


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