290 clinical research coordinator jobs found

Description The Department of Medicine is looking for a motivated individual to join the team at the Center for Neurobiology of Stress and Resilience as a Clinical Research Coordinator. You will coordinate and assist in clinical research studies on neurogastroenterology, including IBS. As a Clinical Research Coordinator, you will be responsible for coordinating and preparing study materials, recruiting potential research subjects, managing research supplies, and assisting with the preparation of study budgets and financial documents. You will also perform patient assessment and symptom management, review research data and enter it into databases, and coordinate clinical research studies, including gastrointestinal endoscopic procedures and tissue collection, hormone challenge studies, blood and salivary samples, treatment trials, bioimpedence testing, and neuroimaging. Finally, you will also act as a liaison between staff and subjects for research coordination, and participate...

Job Description Summary This position will be providing support to the following programs: Pulmonary & Critical Care Clinical Research, COVID-19 Research, and Research in Advanced Therapies in Gastroenterology. Will be responsible for adhering to study guidelines, coordinating study visits, ensuring participants meet stringent clinical inclusion guidelines, provide education to patients and their families. This position may conduct study visits after hours and on weekends for enrollment into the COVID-19 and Critical Care trials. Additionally, incumbent will be responsible for maintaining study database, completing study documents, recruiting study patients, and preparing/conducting monitor and auditor visits. Some travel is required. Entity Medical University of South Carolina (MUSC - Univ) Worker Type Employee Worker Sub-Type​ Research Grant Cost Center CC000974 COM DOM PULM General CC Pay Rate Type Hourly Pay Grade University-05 Pay Range $35,360 - $50,395 - $65,429...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United States of America) Job Summary: Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing required forms and reporting results. Job Description: Essential Responsibilities: 1. Assists in survey development, response tracking, data requests, prepares study materials, and ensures protocol adherence 2. Assists with scheduling research interviews, focus groups and email communications 3. Participates in development and submission of study related documents to the IRB for each assigned study(s) 4. Participates in data analysis, programming, data management, abstracts, data tables, and presentations 5. Assesses potential participant’s (patients and clinicians) eligibility for study inclusion based on protocol(s) 6....

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United States of America) Job Description Summary The Clinical Research Coordinator II will be responsible for the coordination and administration of multiple research studies. Responsible for assigned research studies and general research duties. Implements study protocols in accordance to regulatory and institutional requirements. Works closely with principal investigators, research staff and Research Administration facilitating all aspects of assigned clinical trials. Interacts with study participants diagnosed with various medical conditions and diagnoses. Job Description: 1) Possesses ongoing knowledge of FDA, OHRP and GCP regulations: Ensures adherence to regulations. Educates and mentors other study staff as applicable. 2) Responsible for coordinating different phases of research studies with varying degrees...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United States of America) CLINICAL RESEARCH COORDINATOR is an entry level position requiring a bachelor's degree. This position supports several Principal Investigators and is located in the Research Administration Department of the hospital. Job Description: CLINICAL RESEARCH COORDINATOR FLSA Status: Exempt As a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) and COVID-19 as a condition of employment. Learn more about this requirement. More than 35,000 people working together. Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives. Your skill and compassion can make us...

Fred Hutch is proud to be an Equal Opportunity and VEVRAA Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability, marital or veteran status, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. Read the EEOC Know Your Rights: Workplace Discrimination is Illegal poster here .

Fred Hutch is proud to be an Equal Opportunity and VEVRAA Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability, marital or veteran status, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. Read the EEOC Know Your Rights: Workplace Discrimination is Illegal poster here .

Fred Hutch is proud to be an Equal Opportunity and VEVRAA Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability, marital or veteran status, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. Read the EEOC Know Your Rights: Workplace Discrimination is Illegal poster here .

These positions 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. Oversight of the clinical trials start-up process from receipt of protocols through 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...

Description The David Geffen School of Medicine, Department of Surgery, Division of Liver and Pancreatic Transplant, is seeking to hire a full time Clinical Research Coordinator to function as the Study Coordinator. Under the direction of the Principal Investigator and the Clinical Trials Director, you will complete the following duties: * Research personnel and hospital staff (collectively, the Study Team) to serve as Study Coordinator and Data Manager for research studies by assuring compliance with all aspects of individual studies. * Be responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). * Be responsible for adherence of all relevant regulatory and Good Clinical Practice (GCP) guidelines. * Ensuring the timely coordination and completion of study related procedures...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United States of America) Job Summary: Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing required forms and reporting results. Job Description: Essential Responsibilities: 1. Assists in survey development, response tracking, data requests, prepares study materials, and ensures protocol adherence 2. Assists with scheduling research interviews, focus groups and email communications 3. Participates in development and submission of study related documents to the IRB for each assigned study(s) 4. Participates in data analysis, programming, data management, abstracts, data tables, and presentations 5. Assesses potential participant’s (patients and clinicians) eligibility for study inclusion based on protocol(s) 6....

Description The Clinical Research Coordinator will participate in all research activities as part of the clinical research team located at UCLA Westwood/UCLA Santa Monica while under the direction of the Administrative Staff Manager, the study investigators, Medical Director/ Principal Investigators in the Department of Pediatrics. You will be responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner for all assigned research studies. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). All relevant regulatory and Good Clinical Practice (GCP) guidelines must be adhered to in addition to ensuring the timely coordination and completion of study related procedures for which the coordinator is responsible. Further, this position requires that the individual participate in patient recruitment and enrollment, data collection, source...

Fred Hutch is proud to be an Equal Opportunity and VEVRAA Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability, marital or veteran status, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. Read the EEOC Know Your Rights: Workplace Discrimination is Illegal poster here .

The position is unique in that it will perform both Clinical Research Coordinator and Research Technician work within the clinical research program and support the bench research lab. This position will be responsible for the management of Genitourinary Oncologic patient samples integral with our development of an organoid biobank and to support of our translational research for key clinical trials. Accuracy and attention to detail is critical in recording both the intake of patient samples and their monitoring. This research technician will support the research activities of the Freedman Lab and the Gelb biobank. Supports the Gelb Center research team in the overall conduct of translational research. May assist with clinical data curation. This is an exciting opportunity to be a part of a research team focused on studying cancer genetics and epigenetics in prostate cancer. In addition, the position will also perform Research Technician duties. Located in Boston and the surrounding...

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 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, Dana-Farber...

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 individuals at high-risk of cancer, and biorepository collections. This is an exciting and challenging opportunity for an individual who is motivated to work in an innovative academic center on cutting edge genetics research, and is interested in working directly with patients, providers, and researchers. Responsible for participant recruitment, data reporting and management, collection of source documents, use and development of case report forms, adverse event reporting, filing and archiving of study records, and resolution of data queries Interact with study participants as directed/required by the protocol and/or study team Ensure all study related samples are collected, properly prepared, and shipped...