372 jobs found

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 .

Description Ready to take charge in the world of clinical research? As a Clinical Research Coordinator, you'll be at the forefront of managing the entire journey of research projects, from conception to completion. Your role involves implementing multiple studies, juggling tasks to meet crucial deadlines, and ensuring strict adherence to study protocols and regulations. Collaboration is key as you work alongside the Principal Investigator, various departments, sponsors, and more, ensuring studies run smoothly, stay compliant, and receive the support they need. Join us in shaping the future of clinical research with the department of Rheumatology. Salary: $32.65 - $52.53/hour Qualifications Required: * Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborative relationships. * Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and...

Description To support Clinical Trials, The Department of OBGYN is seeking to hire a full time Clinical Research Coordinator. You will work with the PI, Sub-Investigators, 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. You will be responsible for: * Ensuring that protocol procedures have been completed accurately, safely, and in a timely manner; including the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). * Responsible for all relevant regulatory and Good Clinical Practice (GCP) guidelines which must be adhered to in addition to ensuring the timely coordination and completion of study related procedures for which the coordinator is responsible. * Participation in patient recruitment and enrollment, data collection, source documentation, quality...

The Nurse Clinical Research II will integrate theoretical knowledge with clinical experience in the evaluations and treatments of study subjects along with the attending physician and/or Principal Investigator. This position will function in a team lead role, and use their knowledge of nursing practice and ability to comprehend significant elements based upon previous experience. Essential duties of this position include, but are not limited to, assist with identification and recruitment of research patients, as well as assess, plan, implement and evaluate research related activities while understanding patient medical problems. Data management and documentation related to research subjects and studies will also be important job functions, and this position will ensure the study maintains documentation, and that appropriate team review, ethical approval and study activation is undertaken before patient recruitment begins. Furthermore, this position will evaluate completed case...

Apply Now - External Applicants Apply Now - Current Colleagues Tracking Code 2023-18286 Shift Day Job Location Decatur, Illinois Description Essential Functions and Job Duties Coordinates screening and enrollment of clinical trial patients. Reviews physician patient schedules and assesses patients for possible clinical trial enrollment. Educates patients and families during the informed consent process. Registers patients and participants to protocols. Ensures eligibility requirements are met and reviews with physician investigator. Ensures protocol required patient testing is ordered and complete. Maintains record of recruitment strategies. Markets protocols as needed to meet recruitment goals. Coordinates clinical trial activities research done at the clinic and hospital Gathers and verifies source documents Verifies the accuracy, completeness and timely submission of case report forms. Collaborates with investigator to ensure protocol compliance in patient selection, treatment,...

Description The Semel Institute is seeking to hire a Part Time, Limited Staff Research Associate 1 to complete the following duties: * Laboratory research support * Assist with data management and analysis using SPSS and other programs. * Assist with IRB applications and renewals, correspondence and communications, planning meetings and overseeing timeline(s) for program activities and studies, drive between study sites to coordinate and perform study activities and operations, preparation of manuscripts and other study dissemination products and activities. * Coordinate and distribute gift cards/petty cash and/or complete other participant compensation protocols. May convert to career. Pay Range: $25.75 - $30.71 hourly Qualifications 1.Ability to coordinate data collection and data entry for research studies/program activities across sites. 2.Ability to interact appropriately and congenially with all staff, faculty, students, patients and the public at all...

Description Under the direction of the WHCRU Administrative Director, you will function as a member of the Women's Health Clinical Research Unit in the Department of Obstetrics and Gynecology. You will work with the PI, Sub-Investigators, 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. You'll 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). 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 you participate in...

Description The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. In this role, you will perform necessary tasks to assist in managing projects and prioritizing work to meet necessary deadlines. You will provide support in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations. Hourly Salary Range: $26.29 - $42.28 Qualifications Required: * Ability to work efficiently and complete tasks with thoroughness and accuracy. * Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport and build relationships. * Strong organizational capabilities. * Skills sufficient to solve problems and identify solutions. * Ability to adapt to changing job demands and priorities; work flexible hours to...

Description Join our dynamic team and provide technical and paraveterinary services. Major duties include assisting in Breeding Colony Management, and providing veterinary support services. Salary: $25.75 - $30.71/ hour Qualifications Required: * Knowledge of and ability to accurately follow all SOPs associated with a GLP study, including required study procedures and GLP documentation procedures * Ability to use or learn full capability of word processing software, e-mail, spreadsheets, the internet and other computer programs * Ability to work accurately and with detail * Ability to work as part of a team * Skill in writing clear and concise correspondence * Ability to communicate professionally and courteously on the phone, in person and by e-mail to a variety of people * Excellent interpersonal skills to effectively communicate with faculty and staff that have varying degrees of veterinary medical training * Ability to complete tasks in an orderly and timely...

Description The Semel Institute is seeking to hire a full time Staff Research Associate 1 to complete the following duties: * Working in development of gene editing approach for single enzyme inherited liver disorder. * Editing homologous genome in human pluripotent stem cells. * Maintaining a high level of organization and an orderly lab environment. * Designing of experiments with appropriate experimental and control groups, keeping detailed, accurate records, and the analysis and preparation of data for presentations and publications. * Participate in the preparation of grant applications * Working within a highly interactive team with researchers at all levels of training. After initial training, research duties would be expected to be carried out independently with little or no supervision. Pay Range: $24.88 - $29.67 hourly Qualifications '-University level course work in molecular and cell biology. -Skills in routine molecular and cellular biology...

Description The Department of Medicine is seeking an experienced Staff Research Associate III to join our team. The ideal candidate should possess expertise in various areas, including molecular cloning, the utilization of mouse models for physiological experiments, and advanced microscopy techniques. A minimum of three years of hands-on experience in electron microscopy is highly desirable. In this role, your responsibilities will encompass a range of tasks such as sample preparation for electron microscopy, the creation of blocks suitable for sectioning using Glass and Diatome Diamond Knife, and the formulation of fixatives for cell culture and mouse tissue specimens. You must exhibit proficiency in optimizing electron microscopy protocols for standard transmission electron microscopy, dual-axis electron tomography, and immunogold electron microscopy. Additionally, your proficiency should extend to the realm of cell culture, encompassing mammalian cells and insect cells,...

Description Come join our exceptional Department of Neurobiology, and help lead the advancement of cutting-edge basic science research into explorations of the brain and central nervous system. In this research technician (SRA 2) role you'll work in the nexus of neuroscience research at UCLA, and will: * Perform research on the cortical control of eye movements using animals as models. * Conduct research experiments in accordance with laboratory and safety protocols; this includes: collecting neurophysiological and behavioral data in awake behaving animals, handling the animals, assisting the PI and lab members in surgical procedures, and maintaining surgical implants. * Maintain accurate records of procedures used to conduct experiments. * Use computers to conduct analyses of experimental data. * Provide regular interpretation of analyses and be able to recognize/address issues or problems. * Maintain laboratory equipment, perform or arranges for basic...

Description The Crump Institute is currently seeking a highly motivated Staff Research Associate I to join our research team. As a key member, you will work directly with the Principal Investigator (PI) to provide essential support for general lab activities. These activities include sample processing, performing assays, maintaining cells and corresponding cell assays, as well as recording and analyzing results. The successful candidate for this position will demonstrate an in-depth understanding of laboratory procedures and possess a strong commitment to maintaining a clean and safe workspace. Adherence to all lab regulations pertaining to health and safety is of utmost importance. We are looking for an ideal candidate with expertise in small animal handling and basic in vivo skills, such as tail vein injections (i.v.), intraperitoneal injections (i.p.), oral administrations (p.o.), and intratracheal injections (i.t.). Furthermore, the candidate will assume primary...

Description As the Clinical Research Coordinator for the Department of Medicine, CARE Center, you will be responsible for performing research activities directly related to HIV clinical trials and COVID-19 clinical trials. Duties include: •Coordinate activities for clinical research studies, such as participant recruitment and enrollment; data management; and education as related to each protocol •Document signs, symptoms and other changes with research patients •Assist with preparing reports and submissions •Participate in quality assurance activities for studies across the research unit •Work with outreach team in expanding recruitment efforts for COVID-19 and HIV trials Salary range: $32.65-$52.53 Hourly Qualifications Required: * Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment. * Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. * Ability to...

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...

Current Employees: If you are a current employee, please apply via the internal career site by logging into your Workday Account and clicking the "Career" icon on your homepage. Starting Pay Rate Range $19.07 to $23.84 (Determined by the knowledge, skills, and experience of the applicant.) Job Summary Clinical Research Specialist is responsible for working in collaboration with the Clinical Research team and performing established clinical support for the conduct of clinical research trials. Working under the direction from leadership and the Clinical Research Coordinators to develop, implement and continue evolution of systems that ensure adherence to research protocols, institutional policies, local/state/federal regulations and “Good Clinical Practice.” Establish and maintain effective working relationships with team members, extended Healthcare providers, clinical research organizations, and regulatory agencies to ensure the safe and effective care of...

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 .