- Comprehend study design of each protocol that is 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
- Experience and training in conducting clinical trials with knowledge of ICH GCP
- Licensed Nurse in Missouri
- 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
Clinical Research Coordinator II - Chesterfield, United States - Headlands Research
Description
Overview:
Clinical Research Professionals (CRP) is a dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through the advancement of new drug therapies and medical devices. We have recently partnered with the Headlands Research Network to provide best in class clinical trial services.
This is a full time position based at our office in St. Louis, MO
The Role
Clinical Research Professionals is looking for a Clinical Research Coordinator with a Nursing license to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
Responsibilities: