Clinical Research Coordinator (JH)
A health services organization in Illinois is looking to add a new Clinical Research Coordinator to their growing team in Chicago.
In this role, the Clinical Research Coordinator will be responsible for managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
Responsibilities:
The Clinical Research Coordinator will be responsible for:
Informing participants about study objectives Preparing study materials such as consent forms, brochures, and other written materials for distribution to participants Assisting in recruitment efforts by identifying potential participants Managing the clinical trial process to ensure it complies with regulatory standards and is consistent with ethical principles of human experimentation Coordinating with clinical staff to schedule appointments and ensure that the trial runs smoothly Recording clinical data and results during the study Regulating and monitor the study to make sure protocols and procedures are being followed Managing subject medical records and other data during the study Monitoring multiple research projects and implementing adequate levels of coordination so that all projects are adhering to the conduct of quality research Performing other duties, as needed
Qualifications:
1
year of experience with centralized sponsor driven trial High School Diploma / GED Knowledgeable in Medical terminology Solid understanding of Regulatory requirements, as well as Good Clinical Practices (GCP), HIPAA and International Conference on Harmonization (ICH) guidelines Great interpersonal skills Excellent communication skills (written and verbal) Strong attention to detail Highly organized Desired Skills:
Associate's and/or Bachelor's Degree Recommended Skills Attention To Detail Clinical Research Coordination Clinical Trials Clinical Works Communication Coordinating Estimated Salary: $20 to $28 per hour based on qualifications.
In this role, the Clinical Research Coordinator will be responsible for managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
Responsibilities:
The Clinical Research Coordinator will be responsible for:
Informing participants about study objectives Preparing study materials such as consent forms, brochures, and other written materials for distribution to participants Assisting in recruitment efforts by identifying potential participants Managing the clinical trial process to ensure it complies with regulatory standards and is consistent with ethical principles of human experimentation Coordinating with clinical staff to schedule appointments and ensure that the trial runs smoothly Recording clinical data and results during the study Regulating and monitor the study to make sure protocols and procedures are being followed Managing subject medical records and other data during the study Monitoring multiple research projects and implementing adequate levels of coordination so that all projects are adhering to the conduct of quality research Performing other duties, as needed
Qualifications:
1
year of experience with centralized sponsor driven trial High School Diploma / GED Knowledgeable in Medical terminology Solid understanding of Regulatory requirements, as well as Good Clinical Practices (GCP), HIPAA and International Conference on Harmonization (ICH) guidelines Great interpersonal skills Excellent communication skills (written and verbal) Strong attention to detail Highly organized Desired Skills:
Associate's and/or Bachelor's Degree Recommended Skills Attention To Detail Clinical Research Coordination Clinical Trials Clinical Works Communication Coordinating Estimated Salary: $20 to $28 per hour based on qualifications.
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