208 clinical research coordinator jobs found

Responsibilities In this role, you will serve in a dual role as a Senior Clinical Research Coordinator, Supervisor working directly with Investigators and study teams in managing studies, and CRC Supervisor, overseeing the daily operations of the OCR-CSE Clinical Research Coordinator Team. This dual role will have a title of Sr. CRC Supervisor. In this role, you will independently coordinate and will be accountable for the overall administration of multiple clinical studies and the supervision of the CRC Team, typically requiring advanced-level knowledge and skills.  You may provide leadership to lower-level clinical research coordinators and/or other support personnel.  You will be responsible for, and critically important to the overall operational management of their assigned clinical research activities and will have direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multi-center clinical trials (both...

Responsibilities As the Senior Clinical Research Coordinator you will be primarily responsible for the coordination of research activities under the direct supervision of the Santa Monica Research Operations Manager. You will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, this includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities will include: • Regulatory compliance • Patient recruitment and enrollment • Data collection • Research chart documentation  • Quality assurance • Report preparation  • Protocol information dissemination  You will also meet with staff on an annual basis to develop and implement career goals in order to encourage and promote professional growth and development. Travel to other locations may be required.  Salary range: $5116.67-$10116.67 Monthly Qualifications...

Responsibilities The Division of Pulmonary Medicine is seeking a motivated Clinical Research Coordinator to implement and manage critical care and related pulmonary disease research projects, under the direction of the clinical Principal Investigator (PI). In this role, you will support, facilitate and coordinate the daily clinical trial activities and play a critical role in the conduct of the study. You assist with study initiation procedures, patient screening and recruitment, consenting, surveying, and tracking of the study subjects as outlined in each of the study protocols. You will also be responsible for ensuring adherence to study protocols, accurate and timely collection, review and entering of data into specified electronic data capturing systems while maintaining patient confidentiality. You will work to collect, prepare, store and ship specimens to a central site and develop and maintain research enrollment logs, monitor for adverse events and maintain all...

The Clinical Research Coordinator I will support two large tissue banks run by Dr. Jennifer Brown, Director of the CLL Center and Professor of Medicine. One of these tissue banks enrolls all patients with CLL and collects saliva, blood, and bone marrow, as well as clinical history data on these patients.  The second tissue bank focuses on patients with CLL or other lymphomas who have multiple family members with lymphoma or CLL. As part of this study, the patient is enrolled and many of their family members will be enrolled by mail. This project is undergoing a current push for new enrollment. This Coordinator will work within the lymphoma clinical research program, but the responsibilities will be to support these two tissue banks. This individual will screen patients for tissue bank eligibility, obtain informed consent, and register study participants with the Office of Data Quality (ODQ). Patient contact is required. Located in Boston and the surrounding communities,...

The Pediatric Solid Tumor Program at Dana-Farber Cancer Institute is seeking to hire a motivated and experienced Clinical Research Coordinator (CRC II) to work within the Clinical Translational Research Program (CTIP) on trials specific to the Solid Tumor Biology and research portfolio. The pediatric Solid Tumor Program is one of the largest in the world and treats children with a range of solid tumor diagnoses providing novel and cutting-edge therapies for these rare diseases. The Biology Clinical Research Coordinator will work within the Solid tumor Biology group and specifically Dr. David Shulman’s research program that focuses on the development of novel therapies and liquid biopsy assays.  The CRC will support the research team in the overall conduct of a variety of clinical trials and research projects that focus on the development of novel biomarkers and treatments for solid tumors affecting adolescents and young adults. The CRC’s efforts will primarily be focused on...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the Thoracic clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber...

The Clinical Research Coordinator works within the clinical research program and supports the research team in the overall conduct of health outcomes research using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. While participating collaboratively within the research program on open studies, the CRC’s primary responsibility will be supporting outcome disparities research projects. All research projects within this portfolio will be focused on identifying outcome disparities in childhood cancer and blood disorders, understanding the mechanisms underlying these disparities, and developing and testing interventions to ameliorate disparities. The portfolio includes multi-center survey-based cohort studies, multi-center supportive care intervention studies and correlative biology studies. These studies will include a significant component of patient-facing research, including interacting with newly diagnosed pediatric...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. This position will be based at Dana-Farber Milford and Weymouth campus....

The Clinical Research Coordinator work within the GYN clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...

The Clinical Research Coordinator work within the clinical research program of Thoracic Oncology and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities,...

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. Responsibilities Investigators in the Division of Cancer Genetics and Prevention at the Dana-Farber Cancer Institute seek a full-time Clinical Research Coordinator to assist in clinical and non-clinical research studies related to cancer prevention, genetic testing, early identification of...

The Clinical Research Coordinator work within the  clinical research program for the Center for Head and Neck Oncology  and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the...

The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. Some travel may be required. Located in Boston and the surrounding communities, Dana-Farber Cancer...