Clinical Study Coordinator- Cancer Clinical and Translational Research Office

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...

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...

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: * Responsible for keeping clinical research projects in compliance with the Code of Federal Regulations, Sponsor and System guidelines. * Provide technical support to Principal Investigators. * Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. * Abstract...

GENERAL SUMMARY: + Responsible for keeping clinical research projects in compliance with the Code of Federal Regulations, Sponsor and System guidelines. + Provide technical support to Principal Investigators. + Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. + Abstract...

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...

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...

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...

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...

Description: The Division of Hematology & Oncology in the Department of Internal Medicine at the Henry Ford Hospital & Henry Ford Cancer Institute (HFCI) is currently recruiting a full-time, board-certified Academic Head and Neck Cancer Medical Oncologist for its busy, well-established hospital-based, academic practice, with an established fellowship...

This position will be approximately 32 hours per week with a majority of those hours at our West Bloomfield Hospital location. Candidate must have reliable transportation from Henry Ford Cancer's Detroit location to our West Bloomfield location. This research assistant will help our radiation oncologists manage two exciting new grant-funded projects. This...

Proclinical is working closely with a healthcare organization who is seeking a dedicated Clinical Research Associate to join their team. The successful candidate will play a crucial role in determining study eligibility, obtaining study consent, scheduling study procedure visits, and coordinating the collection and processing of study specimens. This role...

Proclinical is working closely with a healthcare organization who is seeking a dedicated Clinical Research Associate to join their team. The successful candidate will play a crucial role in determining study eligibility, obtaining study consent, scheduling study procedure visits, and coordinating the collection and processing of study specimens. This role...

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...

This position will be approximately 32 hours per week with a majority of those hours at our West Bloomfield Hospital location. Candidate must have reliable transportation from Henry Ford Cancer's Detroit location to our West Bloomfield location. This research assistant will help our radiation oncologists manage two exciting new grant-funded projects. This...

Position Summary Under the supervision of the Director of the Integrative Therapies Program, the research nutritionist works with a team of global researchers on studies related to nutrition and integrative medicine in children with cancer. Employee is responsible for coordinating research studies, along with data management, subject accrual, and...