509 Research jobs

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.

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.

Responsibilities Join our team as a Clinical Research Assistant and participate in all research activities as part of the clinical research team located at UCLA/UCLA Santa Monica and Westwood while under the direction of the team leaders, investigators, Financial Administrative Office, Faculty Director, Medical Director, and Senior Research Director of the Jonsson Comprehensive Cancer Center Clinical Research Unit (JCCC CRU). In this role, you will be responsible for completing the data management of clinical research studies, protocol related tasks, assisting with shipment of specimens, and administrative functions of the oncology research unit, according to good clinical practice, JCCC CRU standard operating policies, and UCLA Institutional Review Board and government regulations. You will be responsible for collection and transcription of research patient data and study related information into research records and assist with maintenance of study patient files. You will...

Responsibilities The Senior Clinical Research Coordinator is primarily responsible for coordination of the research activities in Clinical Research Unit within the Division of Hematology/Oncology under the direction of the investigators, Faculty Director of the JCCC CRU, Disease Site Investigator, and the senior management team (Director of Research, Medical Director, and Director of Finance and Administration). You will be is responsible for ensuring 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). 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. You will participate in patient recruitment and enrollment, data collection, source...

Responsibilities This position will entail a large amount of animal work, including working with immunocompromised mice and cell line xenograft models of human cancer. Duties will include day to day care of animals, inoculating mice with human cancer cell lines, monitoring for tumor growth, oral/IV/IP drug administration. Isolation of biological materials, (DNA, RNA and protein) from precious animal and human tissues, and cell lines as well as the cataloging and management of the resources using relational computer database will be required. You will be responsible for the management and daily use of critical laboratory resources including a frozen human tissue bank and human cell line stocks. In vitro culture of human cancer cell lines is also required. You will be expected to perform nonstandard laboratory techniques to meet the needs of various research projects and troubleshoot existing lab protocols and will also be responsible for the training of students, volunteers and...

Responsibilities As the Senior Clinical Research Coordinator you will be primarily responsible for the coordination of research activities under the direct supervision of the Westwood Translational Clinical Team 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 may include: • Regulatory compliance • Patient recruitment and enrollment • Data collection • Research chart documentation  • Quality assurance • Report preparation  • Protocol information dissemination • Sample management • Budget reviews 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:...

Responsibilities As the Data Entry Specialist, you will participate in all research activities as part of the clinical research team located at UCLA/UCLA Santa Monica while under the direction of the COG Principal Investigator, Lead COG Study Coordinator (team leader), study investigators, Division Chief, and Clinical Research Lead in the Department of Pediatrics.  You are responsible for completing the data management of clinical research studies of all clinical research studies specific to the Division of Pediatric Hematology/Oncology.  This includes responsibility for collection and transcription of research patient data and study related information into research records (CRFs) and assists with maintenance of regulatory files to fulfill research requirements. You will work with study monitors to process and collect accurate data in a timely manner and assist investigators and study coordinators in clinic settings.  You will work flexible hours and/or overtime to meet study...

Responsibilities Within the UCLA Brain Tumor Imaging Laboratory (BTIL) in the Department of Radiological Sciences, the Staff Research Associate (SRA) will assist in conducting the preclinical imaging activities of the Lab.  They will primarily focus on performing molecular biology experiments, growing cell cultures and mouse xenograft work.  The SRA will coordinate the preclinical regulatory activities of the lab, such as prepare and submit initial applications (and subsequent annual renewals and amendments) to the local IACUC, EHS and biosafety committees. They will assist in the establishment of an intracranial tumor mouse model for assessing pre-clinical drug pharmacokinetics and efficacy and monitoring tumor burden with imaging systems.   The SRA also coordinates the logistical and administrative aspects of pre-clinical neuroimaging studies for the Lab where they may prepare samples for molecular and histological characterization. The SRA may maintain xenograft mouse...

Responsibilities The Public Administrative Analyst will manage administrative functions related to ongoing and new research studies. This may include assisting other research assistants within the office in the execution of research projects. The Admin Analyst will develop and maintain standard operating procedures for each research study using approved templates where required. Duties include communicating and coordinating with research entities and all regulatory departments within these entities as well as industry sponsors as needed to manage a clinical trial. You will schedule study participant appointments and serve as the patient liaison to the participating physicians. Working closely with the principal investigator, actively participating in the informed consent process as well as maintaining thorough understanding of study protocol(s) to be able to answer all questions pertaining to the study posed during the informed consent process. You may also prepare...

Responsibilities This new Clinical Research Coordinator will assist the Principal Investigators and Sub-Investigator, on our Outreach Research Program for the Alzheimer’s Disease Neuroimaging Initiative and related research studies. You will assist the investigators on outreach, education, and engagement with underrepresented communities to improve awareness and access to clinical research studies in Alzheimer’s disease and related dementias. This study is recruiting staff who can perform outreach to Black/African American and Asian American and Pacific Islander communities, and enhance recruitment and retention in these communities. You will work closely with the UCLA Easton Center Outreach, Recruitment, and Engagement Core which has a program devoted to the Hispanic/Latinx community. Procedures include blood tests, cognitive testing, lumbar punctures, and brain imaging (MRI, PET) in patients with normal cognition, mild cognitive impairment, and Alzheimer’s disease. Training...

Responsibilities Under the supervision of the Clinical Research Center Administrator, you will provide coordination support for Department of Ophthalmology Clinical Research Center. Clinical Research Center duties include managing the daily aspects of clinical trials and maintaining study records with a primary focus on research imaging studies and other ophthalmic studies as assigned by the Administrator of the Clinical Research Center. Salary range: $18.06-$35.78 Hourly Qualifications Required: Demonstrate exceptional oral and written communication skills including knowledge of medical terminology in order to establish effective working relations with all levels of university staff, faculty, private/federal agencies, and with patients. Demonstrate writing and editing skills to complete lay language and technical documents and correspondence by given deadlines. Demonstrate working knowledge of Microsoft Office (Word, Excel, Outlook, and PowerPoint) and the internet...

Responsibilities Under the supervision of the Clinical Research Center Administrator, you will provide coordination support for Department of Ophthalmology Clinical Research Center. Clinical Research Center duties include managing the daily aspects of clinical trials and maintaining study records with a primary focus on research imaging studies and other ophthalmic studies as assigned by the Administrator of the Clinical Research Center. Salary range: $18.06-$35.78 Hourly Qualifications Required: Demonstrate exceptional oral and written communication skills including knowledge of medical terminology in order to establish effective working relations with all levels of university staff, faculty, private/federal agencies, and with patients. Demonstrate writing and editing skills to complete lay language and technical documents and correspondence by given deadlines. Demonstrate working knowledge of Microsoft Office (Word, Excel, Outlook, and PowerPoint) and the internet...

Responsibilities Under the supervision of the Clinical Research Center Administrator, you will provide coordination support for Department of Ophthalmology Clinical Research Center. Clinical Research Center duties include managing the daily aspects of clinical trials and maintaining study records with a primary focus on research imaging studies and other ophthalmic studies as assigned by the Administrator of the Clinical Research Center. Salary range: $18.06-$35.78 Hourly Qualifications Required: Demonstrate exceptional oral and written communication skills including knowledge of medical terminology in order to establish effective working relations with all levels of university staff, faculty, private/federal agencies, and with patients. Demonstrate writing and editing skills to complete lay language and technical documents and correspondence by given deadlines. Demonstrate working knowledge of Microsoft Office (Word, Excel, Outlook, and PowerPoint) and the internet...

Responsibilities Join our team as a Clinical Research Assistant and participate in all research activities as part of the clinical research team located at UCLA/UCLA Santa Monica and Westwood while under the direction of the team leaders, investigators, Financial Administrative Office, Faculty Director, Medical Director, and Senior Research Director of the Jonsson Comprehensive Cancer Center Clinical Research Unit (JCCC CRU). In this role, you will be responsible for completing the data management of clinical research studies, protocol related tasks, assisting with shipment of specimens, and administrative functions of the oncology research unit, according to good clinical practice, JCCC CRU standard operating policies, and UCLA Institutional Review Board and government regulations. You will be responsible for collection and transcription of research patient data and study related information into research records and assist with maintenance of study patient files. You will...

Responsibilities The UCLA Department of Medicine is seeking a motivated Clinical Research Coordinator to collaborate with the researchers at the Center for Neurobiology of Stress and Resilience in neurogastroenterology including irritable bowel syndrome (IBS) as a clinical research assistant. In this role, you will coordinate, prepare, compile and review study materials, successfully recruit and interview potential research subjects, order, maintain, organize and prepare research supplies. You will also assist in the preparation of Institutional Review Board (IRB), study budgets, contracts, and financial documents for the various studies.  You will also oversee study coordinator assessment and symptom management of patients enrolled in studies, review research data and enter into databases; track subject visits and report progress. A key part of your responsibilities will include recruiting and enrolling study participants into clinical research studies. Finally, as a Clinical...

The Hale Family Center for Pancreatic Cancer Research (https://halecenter.dfci.harvard.edu/) at the Dana-Farber Cancer Institute (https://www.dana-farber.org) is dedicated to accelerating the translation of advancements from research to the clinic to improve pancreatic cancer detection, care, and outcomes. The Hale Center fosters collaboration between clinical, translational, and research experts both internally within the Hale Center and Dana-Farber and externally across the broader biomedical community through both academic and industry partnerships. The Hale Center currently consists of 13 investigators and their laboratories together with dedicated Hale Center staff with a collective breadth of expertise in clinical trials, data sciences & machine learning, epidemiology, immunology, medicinal chemistry, molecular & cellular biology, pathology, and radiology. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing...

The Translational Research Coordinator (TRC) will support the Gastrointestinal (GI) Oncology Translational Research Program in the areas of patient consenting, sample processing, and data collection. The GI Oncology Translational Research Program supports various aspects of research for GI Cancers. This program is a bridge between clinical care and wet lab research and supports “bench to bedside” research. Projects that the program supports include the Hale Center for Pancreatic Research (https://halecenter.dfci.harvard.edu/), the OPTISMISTICC Research team through the Cancer Grand Challenges (https://cancergrandchallenges.org/teams/optimisticc), the Lustgarten Dedicated Research Lab (https://lustgarten.org/research/our-lab/), and many more innovative research projects. Duties include the facilitating consent to various GI Oncology Biobanking research protocols, processing blood samples for storage in the GI Biobank, and clinical data abstraction/monitoring of patient statuses. The...

The Translational Research Coordinator (TRC) will support the Gastrointestinal (GI) Oncology Translational Research Program in the areas of patient consenting, sample processing, and data collection. The GI Oncology Translational Research Program supports various aspects of research for GI Cancers. This program is a bridge between clinical care and wet lab research and supports “bench to bedside” research. Projects that the program supports include the Hale Center for Pancreatic Research (https://halecenter.dfci.harvard.edu/), the OPTISMISTICC Research team through the Cancer Grand Challenges (https://cancergrandchallenges.org/teams/optimisticc), the Lustgarten Dedicated Research Lab (https://lustgarten.org/research/our-lab/), and many more innovative research projects. Duties include the facilitating consent to various GI Oncology Biobanking research protocols, processing blood samples for storage in the GI Biobank, and clinical data abstraction/monitoring of patient statuses. The...