American Vision Partners
Jr. Clinical Research Coord
American Vision Partners, Arizona City, Arizona, United States, 85123
Company Intro
At
American Vision Partners (AVP) , we partner with the most respected ophthalmology practices in the country and integrate best-in-class management systems, operational infrastructure, and advanced technology to provide the highest quality patient care possible. Our practices include Barnet Dulaney Perkins Eye Center, Southwestern Eye Center, Retinal Consultants of Arizona, M&M Eye Institute, Abrams Eye Institute, Southwest Eye Institute, Aiello Eye Institute, Moretsky Cassidy Vision Correction, Wellish Vision Institute, West Texas Eye Associates and Vantage Eye Center. We are focused on building the nation's largest and most comprehensive eye care practices and currently operate more than 100 eye care centers in Arizona, New Mexico, Nevada, California and Texas - including 25 ambulatory surgical centers.
At AVP we value teamwork, providing exceptional experiences, continuous improvement, financial strength, and hard work. We are committed to providing best-in-class patient care, pioneering research and technology, and most importantly, rewarding and recognizing our employees!
Overview
As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.
Responsibilities
Acts as a representative of clinical research and as liaison between investigators, other study staff, primary care providers, IRB and sponsor.Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses' oversight for help with clinical decision making.Responsible for all data and source documentation, and adverse experience reportingResponsible for following departmental policiesResponsible and for assuring proper billing for research subjects. Assures that charges for tests and treatments are appropriately communicated and processed.Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed.Attends study-related meetings as appropriate.Travels between RCA research offices as needed for patient and business needs.Develops screening/enrollment/follow up mechanisms.Ensure adherence to protocol requirements.Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable.Organizational maintenance of all aspects of the trial, including but not limited to timeliness in completing CRFs, reporting adverse events, managing caseload and study files.Responsible for quality data entry into sponsor's database (electronic data capture systems or paper CRFs) and query resolution.Ensures proper study drug administration, compliance and accountability, including receipt and , storage and dispensing.Ensures patient safety and ensures coordination of patient care as needed.Assists with maintenance of regulatory documents, IRB reporting and submissions of amendments, renewals, etc.Assists with study initiation visits, monitoring visits, closeout visits and audit visit, ensuring all study documentation and study issues are addressed.Communicates regularly with the Manager of Clinical Research at RII and Principal Investigators about study related issues.Ensures compliance with department standards and all federal regulations and international guidelines of good clinical practice.Maintain job related certifications (IATA, Human subjects, subjects' protection training, GCP, and protocol specific required training).Active in acquiring professional growth by obtaining CRC certification when eligible and joining a professional association such as SOCRA or ACRP.Performs other duties and responsibilities as required.Promotes a positive work environment and works to be an integral member of the teamEncourage a team-oriented environment supporting the AVP Mission, Vision and Core Values.Participate in on-going training and continuing education.Show respect and deal appropriately with co-workers, patients, and visitors.Perform any and all duties assigned.Qualifications
Associate or Bachelor's Degree or working toward oneClinical experience in Retina or other optical carePrior research experienceCurrent IATA, Human Subjects' protection training or GCP training highly desirable
Certificates, Licenses, Registrations:
Specialty certification such as CCRC preferred
Benefits & Perks
Your health, happiness and your future matters! At AVP, we offer everything medical and dental insurance, significant eye care discounts, child care assistance, pet insurance, continuing education funds, 401(k), paid holidays plus PTO, Sick Time, opportunity for growth, and much more!
At
American Vision Partners (AVP) , we partner with the most respected ophthalmology practices in the country and integrate best-in-class management systems, operational infrastructure, and advanced technology to provide the highest quality patient care possible. Our practices include Barnet Dulaney Perkins Eye Center, Southwestern Eye Center, Retinal Consultants of Arizona, M&M Eye Institute, Abrams Eye Institute, Southwest Eye Institute, Aiello Eye Institute, Moretsky Cassidy Vision Correction, Wellish Vision Institute, West Texas Eye Associates and Vantage Eye Center. We are focused on building the nation's largest and most comprehensive eye care practices and currently operate more than 100 eye care centers in Arizona, New Mexico, Nevada, California and Texas - including 25 ambulatory surgical centers.
At AVP we value teamwork, providing exceptional experiences, continuous improvement, financial strength, and hard work. We are committed to providing best-in-class patient care, pioneering research and technology, and most importantly, rewarding and recognizing our employees!
Overview
As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.
Responsibilities
Acts as a representative of clinical research and as liaison between investigators, other study staff, primary care providers, IRB and sponsor.Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses' oversight for help with clinical decision making.Responsible for all data and source documentation, and adverse experience reportingResponsible for following departmental policiesResponsible and for assuring proper billing for research subjects. Assures that charges for tests and treatments are appropriately communicated and processed.Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed.Attends study-related meetings as appropriate.Travels between RCA research offices as needed for patient and business needs.Develops screening/enrollment/follow up mechanisms.Ensure adherence to protocol requirements.Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable.Organizational maintenance of all aspects of the trial, including but not limited to timeliness in completing CRFs, reporting adverse events, managing caseload and study files.Responsible for quality data entry into sponsor's database (electronic data capture systems or paper CRFs) and query resolution.Ensures proper study drug administration, compliance and accountability, including receipt and , storage and dispensing.Ensures patient safety and ensures coordination of patient care as needed.Assists with maintenance of regulatory documents, IRB reporting and submissions of amendments, renewals, etc.Assists with study initiation visits, monitoring visits, closeout visits and audit visit, ensuring all study documentation and study issues are addressed.Communicates regularly with the Manager of Clinical Research at RII and Principal Investigators about study related issues.Ensures compliance with department standards and all federal regulations and international guidelines of good clinical practice.Maintain job related certifications (IATA, Human subjects, subjects' protection training, GCP, and protocol specific required training).Active in acquiring professional growth by obtaining CRC certification when eligible and joining a professional association such as SOCRA or ACRP.Performs other duties and responsibilities as required.Promotes a positive work environment and works to be an integral member of the teamEncourage a team-oriented environment supporting the AVP Mission, Vision and Core Values.Participate in on-going training and continuing education.Show respect and deal appropriately with co-workers, patients, and visitors.Perform any and all duties assigned.Qualifications
Associate or Bachelor's Degree or working toward oneClinical experience in Retina or other optical carePrior research experienceCurrent IATA, Human Subjects' protection training or GCP training highly desirable
Certificates, Licenses, Registrations:
Specialty certification such as CCRC preferred
Benefits & Perks
Your health, happiness and your future matters! At AVP, we offer everything medical and dental insurance, significant eye care discounts, child care assistance, pet insurance, continuing education funds, 401(k), paid holidays plus PTO, Sick Time, opportunity for growth, and much more!