Clinical Research Coordinator
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Job Type
Full-time
Description
Southeast Retina Center, an affiliate of Eye Health America, is a growing, multi-specialty ophthalmology practice.? Our focus is on excellence in patient care and creating an exceptional customer/patient experience. We are always seeking exceptional people who aren't just searching for a job but looking to make a difference.
We are looking for an experienced Clinical Research Coordinator who is familiar with and has a working knowledge of all aspects of clinical research. The ideal candidate has a B.S or a CCRC with a minimum of 2 years of experience. Retina Clinical experience is a plus. Salary commensurate with qualification and experience.
Job Duties:
Coordinate all clinical trial activities and play a key role in the conduct of the study.
Schedule study participant's appointments and serve as the patient liaison to the PI and other participating physicians.
Review and comprehend the protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections.
Possess a thorough knowledge of the informed consent process
Coordinate approval of new study agreements and contracts and develop clinical study budgets based on proposed study protocols
Coordinate with sponsors pre-qualification visits, monitor visits, and study termination visits.
Complete case report forms and respond to data clarification requests in a timely manner.
Attend Investigator meetings that require travel and report pertinent information back to the research team.
Coordinate with PI and department to help ensure that clinical research and related activities are performed in accordance with Federal regulations, and state and sponsoring agency's policies and procedures.
Maintain logs and spreadsheets to track subject information such as subject screening logs and protocol deviation logs, delegation logs.
Coordinate and facilitate monitoring and auditing visits.
Collaborate with the PI and other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed.
Perform specimen processing and shipment of biological specimens.
Assist with study materials including but not limited to, the informed consent document, case report forms (CRFs), enrollment logs, drug/device accountability logs, and closeout documents
Establish and organize study files, regulatory binders, study-specific source documentation, and other materials as required.
Facilitate secure storage of study documents.
Promote the ethical conduct of research
May need to perform other study-related duties as required by the protocol.Estimated Salary: $20 to $28 per hour based on qualifications.
Job Type
Full-time
Description
Southeast Retina Center, an affiliate of Eye Health America, is a growing, multi-specialty ophthalmology practice.? Our focus is on excellence in patient care and creating an exceptional customer/patient experience. We are always seeking exceptional people who aren't just searching for a job but looking to make a difference.
We are looking for an experienced Clinical Research Coordinator who is familiar with and has a working knowledge of all aspects of clinical research. The ideal candidate has a B.S or a CCRC with a minimum of 2 years of experience. Retina Clinical experience is a plus. Salary commensurate with qualification and experience.
Job Duties:
Coordinate all clinical trial activities and play a key role in the conduct of the study.
Schedule study participant's appointments and serve as the patient liaison to the PI and other participating physicians.
Review and comprehend the protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections.
Possess a thorough knowledge of the informed consent process
Coordinate approval of new study agreements and contracts and develop clinical study budgets based on proposed study protocols
Coordinate with sponsors pre-qualification visits, monitor visits, and study termination visits.
Complete case report forms and respond to data clarification requests in a timely manner.
Attend Investigator meetings that require travel and report pertinent information back to the research team.
Coordinate with PI and department to help ensure that clinical research and related activities are performed in accordance with Federal regulations, and state and sponsoring agency's policies and procedures.
Maintain logs and spreadsheets to track subject information such as subject screening logs and protocol deviation logs, delegation logs.
Coordinate and facilitate monitoring and auditing visits.
Collaborate with the PI and other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed.
Perform specimen processing and shipment of biological specimens.
Assist with study materials including but not limited to, the informed consent document, case report forms (CRFs), enrollment logs, drug/device accountability logs, and closeout documents
Establish and organize study files, regulatory binders, study-specific source documentation, and other materials as required.
Facilitate secure storage of study documents.
Promote the ethical conduct of research
May need to perform other study-related duties as required by the protocol.Estimated Salary: $20 to $28 per hour based on qualifications.
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