Clinical Research Coordinator - Neurology
Position Number: DCRCNEURO
Location: ASRI at Allegheny General Hospital
Department: Neurology
Status: Full-time, 40 hours per week
The Allegheny Health Network is comprised of eight hospitals: Allegheny General, Allegheny Valley, Canonsburg, Forbes, Jefferson, Saint Vincent, Westfield Memorial and West Penn; and more than 200 primary- and specialty-care practices. And we have approximately 1,700 physicians in every clinical specialty, 17,000 employees and 2,000 volunteers. Together, we provide world-class medicine to patients in our communities, across the country and around the world.
Since 1885, Allegheny General Hospital (AGH) has offered medical care to Pittsburgh and its surrounding areas. What started with just 50 beds inside two adjoining brick homes has evolved into a premier health care institution with over 600 beds. Today, AGH still follows the founding partners mission statement, Erected for the benefit of mankind to save life, relieve suffering and conserve health by continually striving for outstanding patient experience and care. Allegheny General offers its patients many modern-day amenities, state-of-the art surgical suites, innovative technology, and advanced medical treatments, which are delivered by its world-renowned doctors in conjunction with exceptional teams of nurses, technicians, clinicians and supporting staff.
Job
Summary:
Plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources. Maintains compliance with all regulatory bodies associated with human subject research.
Job
Responsibilities:
Interfaces with clinical staff to identify patients eligible for clinical trials.
Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study.
Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure that they are informed prior to obtaining written consent.
Completes required follow-up and active patient monitoring per study protocol.
Collects, maintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies.
Plans, coordinates, and manages all activities pertinent to the specific clinical trials, ensuring patient safety, good clinical practices, and compliance with the protocol and regulatory agencies.
Performs other duties as assigned or required.
Qualifications:
Associate's degree, RN, or equivalent research experience. Bachelor's degree preferred.
Generally has at least 2 years of experience.
Driver's license may be required depending on facility requirements.
Current research-related certification from accredited program (e.g. CIRA, CCRP) and/or willing to obtain.
Has mastered the components of clinical research operations and is primarily responsible for independent interactions with patients and sponsors (e.g. study accruals, protocol adherence, regular communication with clinic staff); has frequent and direct line of communication to PIs.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
Location: ASRI at Allegheny General Hospital
Department: Neurology
Status: Full-time, 40 hours per week
The Allegheny Health Network is comprised of eight hospitals: Allegheny General, Allegheny Valley, Canonsburg, Forbes, Jefferson, Saint Vincent, Westfield Memorial and West Penn; and more than 200 primary- and specialty-care practices. And we have approximately 1,700 physicians in every clinical specialty, 17,000 employees and 2,000 volunteers. Together, we provide world-class medicine to patients in our communities, across the country and around the world.
Since 1885, Allegheny General Hospital (AGH) has offered medical care to Pittsburgh and its surrounding areas. What started with just 50 beds inside two adjoining brick homes has evolved into a premier health care institution with over 600 beds. Today, AGH still follows the founding partners mission statement, Erected for the benefit of mankind to save life, relieve suffering and conserve health by continually striving for outstanding patient experience and care. Allegheny General offers its patients many modern-day amenities, state-of-the art surgical suites, innovative technology, and advanced medical treatments, which are delivered by its world-renowned doctors in conjunction with exceptional teams of nurses, technicians, clinicians and supporting staff.
Job
Summary:
Plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources. Maintains compliance with all regulatory bodies associated with human subject research.
Job
Responsibilities:
Interfaces with clinical staff to identify patients eligible for clinical trials.
Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study.
Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure that they are informed prior to obtaining written consent.
Completes required follow-up and active patient monitoring per study protocol.
Collects, maintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies.
Plans, coordinates, and manages all activities pertinent to the specific clinical trials, ensuring patient safety, good clinical practices, and compliance with the protocol and regulatory agencies.
Performs other duties as assigned or required.
Qualifications:
Associate's degree, RN, or equivalent research experience. Bachelor's degree preferred.
Generally has at least 2 years of experience.
Driver's license may be required depending on facility requirements.
Current research-related certification from accredited program (e.g. CIRA, CCRP) and/or willing to obtain.
Has mastered the components of clinical research operations and is primarily responsible for independent interactions with patients and sponsors (e.g. study accruals, protocol adherence, regular communication with clinic staff); has frequent and direct line of communication to PIs.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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