Qureos Mentor

Cedars-Sinai

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 Job Description
 
 
 
 
 Make a difference every single day!
 
 
 
 At Cedars-Sinai, the work you do every day directly affects others' lives. Our passionate and dedicated culture has earned us six Magnet designations for nursing excellence. Join us and experience why U.S. News &amp; World Report recognizes us as one of America's Best Hospitals!
 
 
 Millions struggle with endocrine problems. At Cedars-Sinai, our world-class endocrinologists deliver outstanding care for diabetes, thyroid disorders, adrenal disease and even rare conditions. Trust us to help you feel your best and achieve successful treatment.
 
 
 The Nurse Practitioner - Endocrinology Clinic is responsible for providing specialized clinical care to patients with diabetes and related metabolic illnesses. The role centers on assessment, diagnosis, treatment, education, and continuous management of individuals with Type 1, Type 2, and gestational diabetes, as well as prediabetes, obesity, and connected comorbidities. The NP will work in partnership with physicians and multidisciplinary teams to improve glycemic control, reduce complications, and advance patient outcomes using evidence-supported practice and patient-focused care. Opportunities to contribute to general endocrinology patient care are available should the NP be interested.
 
 
 
 Responsibilities:
 
 
 
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 Perform comprehensive patient assessments, including medical history, physical examination, and risk evaluation.
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 Diagnose and manage diabetes and related metabolic disorders.
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 Develop and implement personalized care plans and individualized treatment plans, including medication management and lifestyle interventions.
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 Implement and evaluate treatment plans, adjusting as necessary to achieve efficient patient outcomes.
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 Prescribe and adjust medications, including insulin and non-insulin therapies, in accordance with state regulations and within scope of practice.
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 Monitor and interpret laboratory results (e.g., A1C, glucose levels, lipid profiles) to track patient progress.
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 Manage acute and chronic complications of diabetes (e.g., neuropathy, nephropathy, cardiovascular risk).
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 Provide education and counseling to patients and their families on disease management, medication adherence, lifestyle modifications, and diabetes self-management.
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 Assist with continuous glucose monitoring (CGM) and insulin pump management when applicable and within scope of practice.
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 Conduct follow-up visits to evaluate treatment effectiveness and patient adherence.
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 Collaborate with endocrinologists, physicians, dietitians, diabetes educators, pharmacists, and other healthcare professionals to deliver comprehensive care.
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 Coordinate referrals to specialists as needed (e.g., ophthalmology, podiatry, cardiology).
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 Participate in multidisciplinary case reviews, care planning, and quality improvement initiatives to enhance patient care and clinical practices.
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 Assist in prior authorizations, denial letters, and conduct 1:1 calls with insurance as needed.
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 Ensure continuity of care across outpatient and inpatient settings when applicable.
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 Stay current with the latest advancements in diabetes care and endocrinology.
 
 
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 Qualifications
 
 
 
 
 
 
 Education:
 
 
 
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 Master of Nursing Degree.
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 Graduate of an accredited Nurse practitioner program approved by the California Board of Registered.
 
 
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 Experience:
 
 
 
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 One (1) plus years&rsquo; experience as Nurse Practitioner with a background in endocrinology or diabetes treatment.
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 Experience managing diabetes devices such as continuous glucose monitors (CGMs) and insulin pumps highly preferred.
 
 
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 Licensure/Certifications Requirements:
 
 
 
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 CA RN License.
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 Nurse Practitioner and Furnishing License.
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 National Certification or eligibility for certification as a Nurse Practitioner.
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 DEA License (schedule 2-5).
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 Basic Life Support Certification
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Nurse Practitioner (NP) - Endocrinology Clinic - Full Time - 8hr Days

<div>
 
 Job Description
 
 
 
 Align yourself with an organization that has a reputation for excellence! Cedars-Sinai was awarded the National Research Corporation&rsquo;s Consumer Choice Award 19 times for providing the highest-quality medical care in Los Angeles. We also were awarded the Advisory Board Company&rsquo;s Workplace of the Year. This annual award recognizes hospitals and health systems nationwide that have outstanding levels of employee engagement. We offer an amazing benefits package that includes health care, paid time off, and a 403(B). Join us! Discover why U.S. News &amp; World Report has named us one of America&rsquo;s Best Hospitals.
 
 
 
 What will you be doing in this role?
 
 
 
 Performing specialized health information activities necessary to organize, maintain and use electronic and paper patient health records in Los Angeles. Depending on area assigned, may specialize in one or more clerical functions, such as coding clerical support, transcription processing and interface. Coordination of record request, image scanning quality auditing, or serve as the satellite rep in off-campus locations. Analyze/research errors. Participate in quality reviews. Compile and trend data and generate reports. Queries multiple electronic records and tracking systems. Understands chart organization and content, CSMC and external requirements related to chart documentation and privacy. Also, performs as a backup for prepping and scanning records as needed, to meet department goals.
 
 
 
 Qualifications
 
 
 
 
 Requirements:
 
 
 
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 High School Diploma or GED required. Associate&rsquo;s degree or some college preferred.
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 A minimum of 2 years&rsquo; experience in a health care setting or related field, preferred.
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 Basic medical terminology required.
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 Registered Health Info Tech (RHIT) preferred.
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 Document imaging experience a plus.
 
 
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 Why Work Here?
 
 
 
 Beyond outstanding employee benefits including health and dental insurance, paid vacation, and a 403(b), we take pride in hiring the best employees. Our accomplished staff reflects the culturally and ethnically diverse community we serve. They are proof of our dedication to creating a dynamic, inclusive environment that fuels innovation.
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Health Info Associate I - Document Imaging

<div>
 
 Job Description
 
 
 
 
 Grow your career at Cedars-Sinai!
 
 
 
 The Angeles Clinic &amp; Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all our patients with cancer.
 
 
 
 Join our team and contribute to groundbreaking research.
 
 
 
 This position functions as a Clinical Research Coordinator providing support for clinical research protocols for the department. The Clinical Research Coordinator will assist the Research Department with all aspects of clinical research. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements.
 
 
 
 Primary Duties &amp; Responsibilities
 
 
 
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 Perform accurate processing of research laboratory specimens while demonstrating a moderate degree of proficiency and understanding of research protocol and laboratory procedures, including centrifuging, aliquoting, storing, and shipping of specimens.
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 Monitor deliveries from sponsor, including inventory of kits, unpacking, and storing of supplies, and using kits and supplies appropriately for specimen collection, processing, storage, and shipping, as mandated by sponsor. Maintain electronic record of supplies.
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 Responsible for administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE&rsquo;s and source documents.
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 Facilitates screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
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 Coordinates logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
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 Responsible for accurate and timely data collection, documentation, entry and reporting, including timely response to sponsor queries.
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 Schedules and participates in monitoring and auditing activities to ensure compliance, including implementing any corrective actions.
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 Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
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 Works closely with investigators and regulatory staff or directly with Institutional Review Board (IRB) to submit adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
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 Acts as a liaison with pharmaceutical company representatives or other project funding organizations to monitor and update project progress.
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 Provides assistance with research finance billing, including identifying and classifying routine care vs. research related care.
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 Attends meetings and conferences related to research activities, including research staff meetings. Participates in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested.
 
 
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 Qualifications
 
 
 
 
 Educational Requirements:
 
 
 
 <ul>
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 High School Diploma or GED required.
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 Associate degree or college coursework in a related field (e.g., Life Sciences, Health Sciences, or similar) preferred.
 
 
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 </ul>
 
 Licenses/Certification:
 
 
 
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 Current Certified Phlebotomy Technician I (CPT I) license issued by the State of California required. (Please note your license number in your resume and application)
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 Current Basic Life Support (BLS) certification from the American Heart Association or American Red Cross required. (Certification must be valid for at least 60 days beyond anticipated start date)
 
 
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 Experience:
 
 
 
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 Minimum of six (6) months of healthcare-related or clinical research experience required.
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 Phlebotomy and/or laboratory assistant experience with demonstrated proficiency in applicable job responsibilities.
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 One (1) year of experience as a Clinical Research Coordinator, Clinical Research Associate, or Clinical Research Assistant preferred.
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 This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time.
 
 
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 #Jobs-Indeed
 
 
</div>

Clinical Research Coordinator I, Laboratory + CPT - The Angeles Clinic & Research Institute

<div>
 
 Job Description
 
 
 
 Working under direct supervision, the Research Associate I performs a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. Assists in general laboratory activities, including maintenance of reagents and stocking of supplies. Files and monitors documents. Keeps accurate and detailed records of experiments and results. Assists in the operation of specialized equipment and machinery. Observes safety standards and procedures. The Research Assistant I will be able to perform routine cellular, micro- and molecular biology procedures including, but not limited to Western, Northern blot, DNA/RNA, PCR, protein extraction, cell culture, Immunohistochemistry, and staining. This position does not have supervisory responsibilities.
 
 
 
 Primary Duties And Responsibilities
 
 
 
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 Performs a variety of routine laboratory tasks and procedures.
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 Keeps accurate and detailed project records of experiments and results.
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 May assist with animal husbandry.
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 Maintains lab equipment and related records.
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 Transports, processes and logs samples.
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 Maintains computer database with relevant clinical information.
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 Performs lab maintenance duties, including glassware cleaning and sterilization.
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 Maintains stocks of general lab materials, and places orders for lab equipment and supplies.
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 Assists new students and fellows at the laboratory.
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 Assists in the operation of specialized equipment and machinery.
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 Observes and complies with safety standards and procedures.
 
 
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 </ul>
 
 Department-Specific Responsibilities
 
 
 
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 Assist with rodent surgeries and electrophysiological and behavioral recordings in models of neural injury/ stroke.
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 Support setup and refinement of new platforms for mouse motor behavior recordings and mouse stroke models.
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 Assist with intracranial recordings in mice and rats during stroke recovery, as well as EEG recordings for seizure monitoring.
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 Perform perfusion, histology, and tissue staining for stroke volume assessment and viral expression analysis.
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 Assist with electrophysiological data analysis, including spike sorting, behavioral kinematic analysis, and DeepLabCut-based automated pose estimation.
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 Serve as the lab's Controlled Substance (CS) designee, coordinating with Comparative Medicine to maintain CS inventory logs.
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 Assist with IACUC compliance activities and serve as the primary liaison with Comparative Medicine for routine inspections.
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 Represent the lab in Environmental Health &amp; Safety (EHS) matters, including monthly safety meetings.
 
 
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 </ul>
 
 
 
 Qualifications
 
 
 
 
 
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 Minimum Requirement: Bachelor&rsquo;s degree in a science-related field.
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 Preferred: Prior experience supporting rodent surgical procedures, electrophysiological and behavioral recording techniques, and laboratory compliance activities.
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 </ul>
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Research Associate I, Gulati Lab

<div>
 
 Job Description
 
 
 
 
 Join us as we translate today's discoveries, into tomorrow's medicine!
 
 
 
 Regenerative medicine is a new and developing field that strives to restore function in diseased or aged tissues through either revitalizing existing cells or transplanting new ones. At the Board of Governors Regenerative Medicine Institute, researchers are turning stem cells into therapies for treating a multitude of prevalent diseases and conditions. We're also exploring how to prevent diseases, and we're extending our knowledge to students in Los Angeles and researchers around the world. To learn more, please visit Board of Governors Regenerative Medicine Institute | Cedars-Sinai
 
 
 
 Are you ready to be a part of breakthrough research?
 
 
 
 The Clinical Research Associate I will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Additionally, this position will include animal work (injections, dissections, and surgery), sample processing, and cell culture.
 
 
 
 Primary Job Duties and Responsibilities:
 
 
 
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 Completes Case Report Forms (CRFs).
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 Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
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 Provides supervised patient contact or patient contact for long term follow-up patients only.
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 Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
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 Assists with clinical trial budgets.
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 Assists with patient research billing.
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 Schedules patients for research visits and research procedures.
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 Responsible for sample preparation and shipping and maintenance of study supplies and kits.
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 Maintains research practices using Good Clinical Practice (GCP) guidelines.
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 Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
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 Participates in required training and education programs.
 
 
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 Department-Specific Duties and Responsibilities:
 
 
 
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 Performs data searches and other related administrative tasks.
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 Assists with research protocol writing and development.
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 Transportation of research medications.
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 Performs study related assessments and questionnaires.
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 Assists with prescreening of potential research participants for various clinical trials.
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 Maintains organized paper and electronic research files.
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 Performs all data collection and data entry tasks for department clinical trials.
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 Assists with preparing manuscripts, letters, and other research documents as needed.
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 Responds to sponsor&rsquo; inquiries regarding protocol start-up activities and recruitment.
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 Performs literature reviews.
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 Attends research meetings and monthly conference calls with sponsors for study updates.
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 Performs cell culture, immunohistochemistry including processing of samples.
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 Performs animal injections, dissections and surgery.
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 Assists with scheduling of visits and assessments.
 
 
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 </ul>
 
 
 
 Qualifications
 
 
 
 
 
 
 Education:
 
 
 
 <ul>
 <li>
 High School Diploma or GED is required.
 
 
 </li>
 </ul>
 
 Experience and Skills:
 
 
 
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 Clinical Research related experience is preferred.
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 Ability to interpret and apply knowledge of State, Federal, and Agency standards to follow regulations.
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 Must possess digital literacy, including Word and Excel, and the ability to use standard office equipment is required.
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Clinical Research Associate I - Regenerative Medicine Institute