Clinical Study Coordinator-Full time

+ Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. + Provide technical support to Principal Investigators. + Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. + Abstract medical information from various...

* HIV Status Neutral Support Coordinator at the Ruth Ellis Center (Research Coordinator) The Ruth Ellis Center (REC) is a community center for LGBTQ+ young people in Highland Park, MI. Since 2016, Henry Ford Health has been collaborating with REC to provide medical services in REC's Health and Wellness Centers. Services include primary care, gender...

GENERAL SUMMARY: * Under minimal supervision of the Translational Center study team, works independently to coordinate translational research projects in both the clinic and laboratory setting, in compliance with the Code of Federal Regulations. * Provides technical support to Principal Investigators, analyzes protocol specific requirements and implements...

GENERAL SUMMARY: + Under minimal supervision of the Translational Center study team, works independently to coordinate translational research projects in both the clinic and laboratory setting, in compliance with the Code of Federal Regulations. + Provides technical support to Principal Investigators, analyzes protocol specific requirements and implements...

GENERAL SUMMARY: Under minimal supervision the Clinical Study Coordinator will: * Coordinates clinical research projects in compliance with the Code of Federal Regulations. * Provide technical support to Principal Investigators. * Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient, and clinician...

GENERAL SUMMARY: Under minimal supervision the Clinical Study Coordinator will: · Coordinates clinical research projects in compliance with the Code of Federal Regulations. · Provide technical support to Principal Investigators. · Analyze protocol specific requirements and implement quality assurance measures to...

Provide experienced study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment as well as providing training and mentoring to team members as required. Manage supervisor responsibilities as required. This position is integral to the overall efficient operation of the CTO. Facilitate...

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: * Assure all study requirements are met and documented and meet both internal and external regulations in accordance...

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: * Assure all study requirements are met and documented and meet both internal and external regulations in accordance...

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: * Assure all study requirements are met and documented and meet both internal and external regulations in accordance...

GENERAL SUMMARY: Under minimal supervision the Clinical Study Coordinator will: · Coordinates clinical research projects in compliance with the Code of Federal Regulations. · Provide technical support to Principal Investigators. · Analyze protocol specific requirements and implement quality assurance measures to...

What We Do Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies. Who We...

Position Summary: Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Independently manage a variety of assignments (including complex, early phase and multifaceted studies) as well as provide training and mentoring to KCI research team members. Function as primary support...

Up to $25,000 Sign on Bonus, based on amount of relevant experience** Unit Specializes in: 4 west is a cardiac telemetry unit designated for the care of the acutely ill adult patient with a variety of diagnoses. Whether it is assisting to manage chronic illnesses or help treat acute conditions, our collaborative team lives to serve our Community and strives...

GENERAL SUMMARY: Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. + Provide technical support to Principal Investigators. + Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. + Abstract medical...

Professorremote typeOn CampuslocationsWilliam Paterson Universitytime typeFull timejob requisition idR327Thank you for your interest in working at William Paterson University.Reporting to the Music Department Chair, this 10-month Coordinator of Jazz Studies faculty position is a fulltime tenure track or fulltime non-tenure track position, with full benefits,...

GENERAL SUMMARY: Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. * Provide technical support to Principal Investigators. * Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. * Abstract medical information...

GENERAL SUMMARY Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from...

GENERAL SUMMARY: Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from...

Administrative Assistant I - Physician Assistant Studies Wayne State University is searching for an experienced Administrative Assistant I - Physician Assistant Studies at its Detroit campus location. Wayne State is a premier, public, urban research university located in the heart of Detroit, Michigan where students from all backgrounds are...