521 jobs found

The Nurse Clinical Research II will be instrumental to the success of clinical trials at the University, and will lead evaluations and treatments of study subjects along with the attending physician and/or Principal Investigator. Essential duties of this position include, but are not limited to, assuming responsibility for identification and recruitment of research patients, as well as assessing, planning and implementing research related activities while using a wide repertory of assessment tools to determine the research patient’s needs. In addition, this position will evaluate the effectiveness of nursing care that is planned, administered or delegated. Complete data management and compliance related to research subjects and studies will also be important job functions, and this position will ensure data collection and entry is completed as well as accurately reported. The Nurse Clinical Research II will also analyze research teams’ performance in relation to study data...

Responsibilities The Clinical Research Associate 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 include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. You will ensure investigational product is adequately managed and documented. Salary range: $24.28-$48.04 Hourly Qualifications Required:  • Demonstrated clinical research experience, including working knowledge of good clinical practices for clinical research. • Ability to work in more than one environment, travel to participating hospitals, and attend off site staff meetings, conferences and investigator...

Responsibilities The Clinical Research Associate 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 include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. You will ensure investigational product is adequately managed and documented. Salary range: $24.28-$48.04 Hourly Qualifications Required:  • Demonstrated clinical research experience, including working knowledge of good clinical practices for clinical research. • Ability to work in more than one environment, travel to participating hospitals, and attend off site staff meetings, conferences and investigator...

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 The Clinical Research Associate 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 include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. You will ensure investigational product is adequately managed and documented. Salary range: $24.28-$48.04 Hourly Qualifications Required:  • Demonstrated clinical research experience, including working knowledge of good clinical practices for clinical research. • Ability to work in more than one environment, travel to participating hospitals, and attend off site staff meetings, conferences and investigator...

Responsibilities This position will support the Principal Investigator (PI) on a UCLA internal pilot grant, "Initiative to Study Hate."  This is a 15% position that is designed for an undergraduate student that is motivated to learn through research. Duties includes: - assisting the principal investigator in participant outreach, recruitment, and screening. - assisting in project related scheduling. - attending weekly laboratory meetings. - assisting in data collection. - filing study data as instructed. This position may evolve and other duties may be assigned throughout the quarter. Salary range: $16.25-$19.25 Hourly Qualifications Organized and motivated undergraduate student with interest in Research.   * Must be a current UCLA Student.  UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin,...

Responsibilities This position will support the Principal Investigator (PI) on a UCLA internal pilot grant, "Initiative to Study Hate."  This is a 40% position that is designed for a Graduate student that is motivated to learn through research. Duties includes: - assisting the principal investigator in participant outreach, recruitment, and screening. - assisting in project related scheduling. - attending weekly laboratory meetings. - assisting in data collection. - filing study data as instructed. This position may evolve and other duties may be assigned throughout the quarter. Salary range: $18.00-$45.00 Hourly Qualifications Organized and motivated Graduate student with interest in Research. *Must be a current UCLA Student UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or...

Responsibilities The Semel Institute for Neuroscience and Human Behavior is seeking to hire a Staff Research Associate II to join the Kasari Lab. Primary duties include: 1. Responsible for the coordination and implementation of intervention/study activities. 2. Responsible for the oversight of the research project. 3. Train and supervise other research associates, graduate students, and post- doctorates on their research duties. 4. Support the data collection and analysis component to meet grant deliverables. Salary range: $27.09-$43.58 Hourly Qualifications Required: Ability to communicate clearly and effectively, verbally, and in writing, with subjects, staff, and supervisors.  Demonstrate ability to write complex research papers and reports that use correct syntax and grammar, and clearly represent research or grant findings.  Skill in speaking and writing to persons of various social, cultural, economic, and educational...

Responsibilities The Semel Institute for Neuroscience and Human Behavior is seeking to hire a Staff Research Associate II to join the Kasari Lab. Primary duties include: 1. Responsible for the coordination and implementation of intervention/study activities. 2. Responsible for the oversight of the research project. 3. Train and supervise other research associates, graduate students, and post- doctorates on their research duties. 4. Support the data collection and analysis component to meet grant deliverables. Salary range: $27.09-$43.58 Hourly Qualifications Required: Ability to communicate clearly and effectively, verbally, and in writing, with subjects, staff, and supervisors.  Demonstrate ability to write complex research papers and reports that use correct syntax and grammar, and clearly represent research or grant findings.  Skill in speaking and writing to persons of various social, cultural, economic, and educational backgrounds.  Knowledge...

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 Under the direct supervision of the Clinical Trials Administrator, you will perform regulatory research activities and data management for the Institute of Urologic Oncology. In this role, you will work with the PI, Sub-Investigators, research personnel and hospital staff (collectively, the Study Team) to develop and/or conduct clinical trials and clinical research projects funded by industry-sponsors, federal and state agencies, and other non-profit foundations and organizations. You will be responsible for preparing, managing and submitting any required study/regulatory documents, and all required applications and forms, including but not limited to: submissions to the applicable Institutional Review Board (IRB), informed consent form development, required contractual and/or grant related documents, investigational pharmacy applications, other ancillary services applications, FDA IND/IDE/510k/SAE/MedWatch applications and submissions, etc. In addition, you...

Responsibilities Duties and Tasks A. Laboratory research support -Enter and manage data -creen, recruit, and track potential participants -Consent participants -Coordination of activities and communications among sites -Plan and schedule program meetings, assessments, treatment/intervention sessions/contacts -Conduct diagnostic interviews/study/program assessments and complete develop assessment materials/programs (e.g. redcap) -chedule and attend program meetings, develop agendas and minutes - Other support tasks [e.g. ordering and tracking supplies; library/literature reviews/checks; correspondence and program communications; assist with all aspects of submission and follow up processes to the Office of Protection of Research Subjects; coordination across program/project sites; support with program students and volunteers; support with grant or funding agency correspondence, tracking, and preparation of reports; assist with production of manuscripts and presentations;...

Responsibilities The Division of Hematology/Oncology is seeking a skilled Staff Research Associate to provide technical support to members of the research team on a number of projects from the laboratory and to actively collaborate with the Department of Laboratory Animal Medicine participating on current adoptive cell transfer and T-cell engineering studies. Scientific job duties include maintaining various human primary cancer cell lines, genetic engineering and functional characterization of human and murine T cells, PCR, qPCR, Elisa and Flow Cytometry for gene transfer experiments for preclinical related work. Laboratory duties and responsibilities include to regularly to maintain research records, laboratory stocks ordering supplies and consumables for research projects, oversee lab functions maintaining optimal compressed gas levels and proper equipment operation assisting the Lab Coordinator on maintain proper functioning of lab equipment and facilities.    This is a...

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...

Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center.  Please review the following instructions prior to submitting your job application: Provide all of your employment history, education, and licenses/certifications/registrations.  You will be unable to modify your application after you have submitted it. You must meet all of the job requirements at the time of submitting the application.  You can only apply one time to a job requisition.  Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the large...

Description Job Title: Genetic Counselor Department: Oncology FLSA: Non Exempt Position Summary:  Genetic counselor will provide pre-test and post-test counseling to patients referred to the cancer genetics program. Genetic counselor will communicate testing results to referring providers and will make appropriate referrals. Genetic counselor will also update patients with variant reclassifications. Requirements:   Education: Master’s in Genetic Counseling Skills: Strong and effective organization and coordination, ability to identify and effectively resolve issues and navigate challenges required. Strong verbal and written communication skills, (including listening, interpreting, and articulating). Collaborates with staff members, management and physicians. Knowledge of relevant computer software programs; strong ability to comprehend and navigate complex scenarios.  Experience: 2 years of genetic counseling experience Certification: Master’s in Genetic Counseling...

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. The Vice President, Research Operations is a senior administrator within the Dana-Farber Cancer Institute. This executive position is responsible for the research operations of the institute including, but not limited to oversight of DFCIs numerous core facilities and integrative research...

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...