Clinical Research Coordinator II
Posted on Oct 7, 2024 by Cone Health
Greensboro, NC
Research
Immediate Start
Annual Salary
Full-Time
Overview:
The Clinical Research Coordinator II works closely with study subjects and other research staff, and is responsible for the day-to-day clinical research process to collect, compile, document, and analyze clinical research data. Working under general supervision, the position conducts subject follow-up visits, completes clinical tasks, prepares research documentation, reports, and graphs while keeping appropriate logs, tracking participants, and preparing study materials.
Talent Pool: Allied Health
Responsibilities:
Completes clinical tasks (i.e., ECGs, PFTs, phlebotomy, drug administration, etc.) when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
Completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data.
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Mentors and trains Clinical Research Coordinators I and Clinical Research Specialists I & II to ensure an effective and compliant team.
Performs other duties as assigned.
Qualifications:
EDUCATION:
Required: Associate degree with 4 years of Clinical Research experience OR Bachelor's degree with 2 years of clinical research experience
EXPERIENCE:
Required: 6 years (education and/or experience)
LICENSURE/CERTIFICATION/REGISTRY/LISTING:
Required: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification
The Clinical Research Coordinator II works closely with study subjects and other research staff, and is responsible for the day-to-day clinical research process to collect, compile, document, and analyze clinical research data. Working under general supervision, the position conducts subject follow-up visits, completes clinical tasks, prepares research documentation, reports, and graphs while keeping appropriate logs, tracking participants, and preparing study materials.
Talent Pool: Allied Health
Responsibilities:
Completes clinical tasks (i.e., ECGs, PFTs, phlebotomy, drug administration, etc.) when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
Completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data.
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Mentors and trains Clinical Research Coordinators I and Clinical Research Specialists I & II to ensure an effective and compliant team.
Performs other duties as assigned.
Qualifications:
EDUCATION:
Required: Associate degree with 4 years of Clinical Research experience OR Bachelor's degree with 2 years of clinical research experience
EXPERIENCE:
Required: 6 years (education and/or experience)
LICENSURE/CERTIFICATION/REGISTRY/LISTING:
Required: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification
Reference: 200007240
https://jobs.careeraddict.com/post/95950287
Clinical Research Coordinator II
Posted on Oct 7, 2024 by Cone Health
Greensboro, NC
Research
Immediate Start
Annual Salary
Full-Time
Overview:
The Clinical Research Coordinator II works closely with study subjects and other research staff, and is responsible for the day-to-day clinical research process to collect, compile, document, and analyze clinical research data. Working under general supervision, the position conducts subject follow-up visits, completes clinical tasks, prepares research documentation, reports, and graphs while keeping appropriate logs, tracking participants, and preparing study materials.
Talent Pool: Allied Health
Responsibilities:
Completes clinical tasks (i.e., ECGs, PFTs, phlebotomy, drug administration, etc.) when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
Completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data.
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Mentors and trains Clinical Research Coordinators I and Clinical Research Specialists I & II to ensure an effective and compliant team.
Performs other duties as assigned.
Qualifications:
EDUCATION:
Required: Associate degree with 4 years of Clinical Research experience OR Bachelor's degree with 2 years of clinical research experience
EXPERIENCE:
Required: 6 years (education and/or experience)
LICENSURE/CERTIFICATION/REGISTRY/LISTING:
Required: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification
The Clinical Research Coordinator II works closely with study subjects and other research staff, and is responsible for the day-to-day clinical research process to collect, compile, document, and analyze clinical research data. Working under general supervision, the position conducts subject follow-up visits, completes clinical tasks, prepares research documentation, reports, and graphs while keeping appropriate logs, tracking participants, and preparing study materials.
Talent Pool: Allied Health
Responsibilities:
Completes clinical tasks (i.e., ECGs, PFTs, phlebotomy, drug administration, etc.) when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
Completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data.
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Mentors and trains Clinical Research Coordinators I and Clinical Research Specialists I & II to ensure an effective and compliant team.
Performs other duties as assigned.
Qualifications:
EDUCATION:
Required: Associate degree with 4 years of Clinical Research experience OR Bachelor's degree with 2 years of clinical research experience
EXPERIENCE:
Required: 6 years (education and/or experience)
LICENSURE/CERTIFICATION/REGISTRY/LISTING:
Required: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification
Reference: 200007240
Share this job:
Alert me to jobs like this:
Amplify your job search:
Expert career advice
Increase interview chances with our downloads and specialist services.
Visit Blog