512 Research jobs

Under general supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.   The Clinical Research Coordinator will support clinical trials at Carilion Clinic in the Department of Cardiology.  Basic responsibilities include supporting research investigators/physicians with guidance on research policies and processes, enabling successful collaborations with research sponsors, monitoring and tracking study progress, study design assistance, regulatory submission and maintenance, research subject visit management, and any other research-related duties, as necessary. Under the supervision of Research and Development, this position is charged with maintaining compliance with study protocols, guidelines set by governing agencies, and institutional...

Under minimal supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.    Recruit, screen, and enroll eligible study participants. Obtain informed consent from study participants.  Manages completion and submission of study related documentation. Communicates with research sponsor or CRO, local or central IRB, Research and Development, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance.  Assist in monitoring enrollment goals.  Coordinates tasks such as developing informed consents and screening materials, scheduling visits, and acting as a liaison between research participants and the research study team. Collects data from patient charts, medical records, interviews, questionnaires,...

Under general supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.    Recruit, screen, and enroll eligible study participants. Obtain informed consent from study participants. Manages completion and submission of study related documentation. Communicates with research sponsor or CRO, local or central IRB, Research and Development, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance. Assist in monitoring enrollment goals. Coordinates tasks such as developing informed consents and screening materials, scheduling visits, and acting as a liaison between research participants and the research study team. Collects data from patient charts, medical records, interviews, questionnaires,...

Under general supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry-sponsored, grant-funded, or internally-funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.  This position will be assigned to support minimal risk or non-interventional studies, unless assigned to serve in a support function for greater than minimal risk studies that also include a Clinical Research Coordinator. This Clinical Research Assistant will work with the Research and Development team to support projects in the Department of Psychiatry and Behavioral Medicine. The Research Assistant will engage with physicians, staff, and patients to work collaboratively towards research goals. This is a grant-funded position. Under supervision of Principal Investigator, assist in overseeing compliance to research protocols. Assists with completion and submission 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.

The Markey Cancer Center (MCC) is recruiting a Clinical Research Auditor/Monitor for Multi-Center Investigator Initiated Trials. This position performs routine audits of MCC trials, study teams, & research programs in accordance with applicable MCC SOPs, to assess & assure compliance with applicable protocols, CFR, GCP, sponsor requirements, and MCC SOPs utilizing CTMB guidelines. Data monitoring of MCC IITs in accordance with CM&DMP. Review data accuracy and completeness. Perform post audit exit interviews. Prepare audit reports, identifying recommendations and required actions and follow up. Evaluate responses, escalate and resolve. Provide guidance and training. Assist in developing training and education initiatives of MCC research staff. Utilize Knowledge of FDA Guidance Documents, CFR, GCP, NIH, NCI, ORI, & OMB. Assist in the development of and maintain master files of audit and monitoring activities. Assist in the development of CAPA plans. Coordinate audit...

Responsibilities Make a positive impact on one of the nation’s top health systems. Help ensure the efficient delivery of award-winning patient care. Take your professional expertise to the next level. UCan do all this and more at UCLA Health. Under supervision of the Principal Investigator in the Department of Radiology, the Research Associate will design and prepare plans and specifications for projects and related algorithms, coordinate testing of software, and participate in the collection, maintenance and analysis of experimental data.   The incumbent will test the feasibility of the design with consideration of such factors as system effectiveness, reliability and configuration. Will be responsible for the design and engineering for algorithms and performing computer image analysis. Responsible for the implementation, development and testing of mathematical formulations and data analysis. Assemble and evaluate information and prepare reports with respect to design...

Responsibilities The Semel Institute for Neuroscience and Human Behavior is seeking to hire part-time Research Coordinator to join the UCLA Center for Autism Research and Treatment. You will provide support to Dr. Rajarman’s clinical trials team. Primary duties include: -       Assisting with patient intakes -       Managing all regulatory documents for the trial -       Scheduling and organizing visits, recruitment, email correspondence with CRO, IRB. -       Screening potential participants for study PI to determine study eligibility -       Maintaining required subject visit documents including documents with PHI -       Maintaining PI calendar -       Maintaining electronic server files -       Other duties as assigned Salary range: $25.46-$36.47 Hourly Qualifications Knowledge of basic psychiatric terminology to converse with physicians, clinicians, patients and public Working knowledge of various departments, patient related policies and procedures, as well as a...

Responsibilities The incumbent will provide research coordination support for Dr. Anne L. Coleman’s research program, including, but not limited to projects falling under the following themes: (1) examining and addressing disparities in eye care through the use of mobile health (mHealth) applications, (2) multidisciplinary approaches to measuring and evaluating proxies for systemic racism and social determinants of health and their impact on eye health, and (3) exploring initiatives and interventions to improve justice, equity, diversity, and inclusion within ophthalmology, (4) effect of lighting on myopia. The research coordinator will also assist with Dr. Coleman’s other research projects involving ophthalmic epidemiology and the use of secondary databases, in addition to clinical projects utilizing chart reviews and electronic medical records (EMR) data, among others. The research coordinator will be responsible for all IRB related paperwork including annual data review and...

Responsibilities As an Administrator, you will help facilitate administrative and operational activities for our research focused areas. Primary duties include: •Develops, implements and enforces administrative and operational policies and procedures to ensure smooth and efficient research operations including administrative management and direction of research staff and staffing issues. •Liaise on Human Resource related matters and organizational policies that impact our laboratories and ensure that these clients’ questions are being answered and needs are being met.  •Serve as a resource to Research Cores (Sales and Service entities) and provide guidance and advice on enhancements to lab operations, staffing models, and business development. Salary Range: $61,400.00 – $121,400.00/year Qualifications •At least 5 years of experience working in basic science research, operations, and/or project management within an academic medical center is highly preferred •Strong...

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...

Responsibilities In this position, you will serve as a Research Coordinator for clinical trials and research studies performed by faculty in the UCLA Division of Stroke and Vascular Neurology. These include multicenter NIH and company-sponsored trials of novel therapies to prevent first and recurrent stroke, natural history studies of the course of unusual cerebrovascular conditions, and studies of novel imaging and blood work methods to diagnose and characterize stroke. You will facilitate study performance primarily at UCLA Westwood campus, with occasional activities at Olive View-UCLA, Santa Monica-UCLA, and other hospitals on the West Side of Los Angeles. You will schedule follow-up visits and study tests, perform structured interviews, NIH Stroke Scale assessments and data abstraction from medical records. In addition, you will assist study investigators with IRB, FDA, and other regulatory paperwork. Salary range: $27.09-$43.58 Hourly Qualifications REQUIRED:...

Responsibilities 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 you participate in patient recruitment and enrollment, data collection, source documentation, quality assurance, regulatory...

Responsibilities Under the general supervision of the Manager, Operations and Administrative Support Team (OAST) and with direction from the Vice Chair for Research, the Research Administrative Assistant will provide administrative support and operational management services for the basic science, translational and clinical research missions of the Department of Anesthesiology & Perioperative Medicine (DAPM). The primary responsibilities include, but are not limited to: schedule management; coordination of lecture series, conferences, retreats, and other research related meetings or events; coordination with UCLA Facilities and Capital Programs on projects for structural repair, renovation, design and planning of research space; business travel arrangements, itinerary coordination and conference and travel purchasing/reimbursement; space and equipment inventory; and communication with suppliers/vendors/contractors to ensure timeliness, accuracy and effectiveness of...

Responsibilities Provide specialized expertise that helps define excellence in patient care. Elevate our state-of-the-art imaging capabilities. Take your career to a higher level. You can do all this and more at UCLA Health. As a team member of Radiology Physics, you will be responsible for the continued development, implementation, and maintenance of our clinical physics program in support diagnostic imaging modalities across multiple departments throughout UCLA Health. This position has an emphasis on Magnetic Resonance imaging accreditation, safety and education across more than 23 hospital and outpatient MRI clinical sites. You will also support the evaluation and calibration of ionizing imaging equipment, including projectional X-ray, mammography, fluoroscopy, and computed tomography. Other activities will include the assessment and standardization of image quality, shielding design, and radiation dosimetry. This role involves regular interaction with government,...

Responsibilities The Division of Gastroenterology is seeking a motivated candidate to fulfill the roles of a Staff Research Associate. In this position, you will work in the UCLA Microbiome Core directed by Dr. Jonathan Jacobs. The main responsibilities are to perform high throughput DNA/RNA sequencing, anaerobic culture of microbes, and lab maintenance. You will collaborate with other members of the lab and interact with users of the UCLA Microbiome Core. You will also perform lab maintenance and administrative tasks needed to sustain efficient laboratory operations. Salary range: $27.09-$43.58 Hourly Qualifications Required: 1. Educational background in Biological Sciences, BA or equivalent. 2. Ability to organize and present results in an appropriate format. 3. Ability to maintain complete and accurate records. 4. Able to read and understand scientific protocols. 5. Ability to work independently after training. 6. Ability to work in an aseptic environment. 7. Ability...

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...