Clinical Research Coordinator
1 week ago
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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