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In the 2009 U.S. News & World Report rankings, Cedars-Sinai was named one of America´s best hospitals. Of the 4861 U.S. hospitals, only 174 were ranked in at least one specialty. We are located in Beverly Hills close to the heart of Los Angeles.

Job Category: NursingJob Specialty: ResearchPosition Type: Regular-F/TShift Length: 8hrHours: 8:30am - 5pm Days: Monday - FridayShift Type: DayWeekends: As Needed Job Description: Summary of Essential Job Duties:Performs a variety of experimental protocols and procedures to support the objectives of one or more lab research projects in an area of research. Assists in general laboratory maintenance. Understanding of general research objectives. Aptitude to perform routine experimental protocols and procedures. Ability to understand and comply with safety standards and regulations. Understanding of specific research objectives in area of research specialization. Knowledge of current experimental developments by reading current scientific literature. Complete routine tasks on a day-to-day basis. Familiar with overall lab organization. Complies with safety standards and procedures. Knowledge of specialized equipment and material. Knowledge of routine cleaning and maintenance procedures to support the activity of one or more research labs. Will perform basic bench work under close supervision. Data entry. Perform other duties as required.Educational Requirements:BS in Biological Sciences, strongly preferred.Experience:1-2 years experience working in laboratory acquired in college or equivalent.Physical Demands:Laboratory environment. Sitting, standing, walking.

Requirements: - Graduation from a school of nursing is required. Bachelors degree in Nursing (BSN) preferred. - 2 or more years of clinical and/or research experience required. - Clinical research experience preferred. Licensure Credentials:- Must possess current Tennessee State Board of Nursing license if primary residence is Tennessee or a Nurse Licensure Non-Compact state.- Must possess a current State Board of Nursing license in the state of primary residence if the state is a Nurse Licensure Compact state.- Certification in clinical research from the Society of Clinical Research Associates or the Association of Clinical Research Professionals must be obtained within one year of assuming the position.Nurses seeking a greater sense of purpose thrive within the dynamic culture at St. Jude Childrens Research Hospital, where our breakthroughs will benefit the lives of children today and well into the future. Located in Memphis, Tennessee, St. Jude is a premier center for research and treatment of potentially fatal childhood diseases, including cancer and certain blood, genetic, and immunodeficiency disorders. With a mission to advance cures, and means of prevention, for pediatric catastrophic diseases through research and treatment, St. Jude is dedicated to providing unsurpassed patient care and to advancing the health of children through biomedical research. Thinking of a career that makes a difference? Consider these outstanding positions:RN OPPORTUNITIESClinical Research Associate RNOperating under general supervision, this position performs data abstraction, collection, and entry to support clinical research and preparing submission for all reportable events. Duties encompass developing, maintaining, and/or monitoring case report forms and ensuring compliance with prescribed interventions and evaluations of the assigned protocol(s). In addition, this position provides data to the collaborating research organization or study sponsor, prepares data reports, and provides patient care, education, and management. www.stjude.org An Equal Opportunity Employer

Join us, and believe in your career.

Join Scott & White and discover the benefits of a nationally-recognized healthcare organization with plenty of open doors. Our dedication to leading research, lifelong learning and professional mobility provides you with plenty of ways to reach your ideal destination. The choice is easy. Scott & White currently has the following opportunity available:Research Grant WriterTemple, TX You will be in charge of researching, developing, writing and submitting grant proposals to the appropriate public (government) and private (foundations, corporations, organization) funding entities. You will need to work with appropriate staff and management to collect information needed development.Requires a Bachelors degree; Masters preferred. You must have at least 3-5 years of experience in grant writing and reporting in a healthcare setting. You must be knowledgeable in government funding mechanisms and processes, government request for proposals, criteria checklists for assessment of priority scores, as well as private sector grant agencies. Requires excellent writing and editing skills, the ability to prioritize and meet deadlines. You must also be detail-oriented and able to work independently with the ability to successfully procure health care related grant funding and program development. Proficiency in research, interpretation and analyzing diverse data required. Knowledge of federal/state legislature, regulatory and grant funding processes required. Join us, and believe in your career. To learn more about this and other opportunities, visit our careers link at: http://careers.sw.org. Scott & White is a fully integrated health system and is the largest multi-specialty practice in Texas, and the sixth largest group practice in the nation. Scott & White employs more than 775 physicians and research scientists who care for patients covering 25,000 square miles across Central Texas. Scott & White has a 636-bed Level I Trauma acute care facility in Temple, an additional 50-bed Long Term Acute Care Hospital in Texas, another 150-bed acute care hospital in Temple, a 76-bed acute care facility in Round Rock (greater Austin area), and a network of 50 primary and specialty clinics throughout the region.Scott & White is an Equal Opportunity Employer | Tobacco-Free Environment.

Global LifeScience company that leads the market in high tech advances in therapeutics is growing their Clinical Data Team. As such, they are seeking Leadership for their Clinical Data Team. If you are looking to grow your career in a leading edge company, have clinical data, project management and leadership background, I´d like to speak with you. This opportunity is located in Southern California; a VERY generous relocation package is offered for this opportunity.

The purpose of this position is to develop a program of research through designing specific projects for submission to funding agencies, implementing research and demonstration projects in the investigator´s area of specialization.

The purpose of this position is to develop a program of research through designing specific projects for submission to funding agencies, implementing research and demonstration projects in the investigator´s area of specialization and preparing papers reporting research results for presentation to scientific/professional organizations. Essential Functions:- Design, develop, obtain funding for, and lead well defined research, demonstration, and evaluation projects in the investigator´s area of particular expertise to advance knowledge that will improve health and health care delivery.- Develop an ongoing program of research through coordinating a series of research proposals and projects into a logical investigation of a particular research question, topic, or area.- Communicate research results to other scientists, clinicians, professional groups, the media and the community through presentations and publications in scientific and professional journals, books; and public presentations.- Work with partners in the health care system to improve the health of Kaiser Permanente and non-Kaiser Permanente members.- This includes providing technical consulting and professional service to KP, serving on various KP committees and task forces, and soliciting clinical input into research, where appropriate.-Promote a positive, science-focused work culture by assisting in the development of Center policy, providing technical services and consultation, and by helping to define the CHR´s future research agenda, and by maintaining security and confidentiality of research and medical data.-Participate in education by helping to train undergraduate, graduate, and post doctoral students pursuing health and health services research careers.-Provide service to the scientific and professional community through membership on scientific peer review groups and national boards; and consult with local, state, and national voluntary and governmental agencies. Qualifications: Basic Qualifications: -Doctoral degree (e.g., Ph.D., M.D., or Dr.P.H.) in one of the social sciences, medicine, or health care disciplines; -Thorough knowledge of quantitative methods (from mathematics and statistics) for dealing with methodological and analytic problems in the investigator´s substantive area of expertise (e.g., epidemiology, sociology, economics); -Working knowledge of health care organization, policy, practice, and management (to facilitate application of research to medical and health care phenomena); and, -Working knowledge of a standard statistical software library (e.g., SAS or SPSS) and design of relational databases. -Research methods and theory in health-research related discipline.-Substantive knowledge in health-related discipline. Required License, Registration, Certificate, or Professional Affiliation:- Investigators from the academic fields typically hold membership in their respective professional/scientific associations. -Investigators from health care fields typically hold licenses in their respective professions (e.g., M.D., R.N.) as well as membership in scientific associations. -Ability to write and communicate effectively to scientific/technical/lay/clinical audiences; and, -Ability to work in a computerized work environment, including word processing and data processing. -Data analysis and interpretation skills. -Demonstrated leadership ability as evidenced by key leadership role on complex research projects including supervision of research staff -Some experience (e.g., 2 3 years) as co investigator or principal investigator of research projects; -Demonstrated ability to author and co-author publications in national, peer-reviewed scientific journals; and, -Experience in organizing and transmitting the knowledge of their disciplines, such as through teaching at the college or university level as an assistant or associate professor: and, -Experience presenting research findings at national meetings. -2-3 years of U.S. population based research experience -2-3 years of demonstrated experience in grant writing and securing external research funding -2-3 years advanced training in epidemiology, genetic epidemiology, health services research, health economics or a related discipline Preferred Qualifications: -Comprehensive knowledge of quantitative methods (from mathematics and statistics) for dealing with methodological and analytic problems in the investigator´s substantive area of expertise (e.g., epidemiology, sociology, economics); -Thorough knowledge of health care organization, policy, practice, and management (to facilitate application of research to medical and health care phenomena); and, -Thorough knowledge of a standard statistical software library (e.g., SAS, SPSS) and design of relational databases. -Outstanding ability to write and communicate effectively to scientific/technical audiences, as well as clinical and lay audiences; -Specialized skills in the area of a theoretical discipline; and, -Computer programming language(s); -Partnership skills, including communications and negotiations. -Some experience (e.g., 3 to 5 years) pertaining to health related research, theory, and policy; and, -Experience working in or with a health maintenance organization, -Experience with diverse populations.

Join Scott & White and discover the benefits of a nationally-recognized healthcare organization with plenty of open doors. Our dedication to leading research, lifelong learning and professional mobility provides you with plenty of ways to reach your ideal destination. The choice is easy. Post-Doc FellowTemple, TXIn this medical research role, you will provide research and technical assistance in studies and projects conducted by a senior principal investigator. You are expected to apply advanced knowledge in the performance of independent research activities and may directly supervise other research personnel in those activities. Requires a Doctorate and some experience in the research field. Join us, and believe in your career. To learn more about this and other opportunities, visit our careers link at: http://careers.sw.org. Scott & White is a fully integrated health system and is the largest multi-specialty practice in Texas, and the sixth largest group practice in the nation. Scott & White employs more than 775 physicians and research scientists who care for patients covering 25,000 square miles across Central Texas. Scott & White has a 636-bed Level I Trauma acute care facility in Temple, an additional 50-bed Long Term Acute Care Hospital in Texas, another 150-bed acute care hospital in Temple, a 76-bed acute care facility in Round Rock (greater Austin area), and a network of 50 primary and specialty clinics throughout the region.Scott & White is an Equal Opportunity Employer | Tobacco-Free Environment.

MGH: Make Greatness Happen

Incumbent serves as a member of the staff of the Research Space Management Group and is responsible for identifying and evaluating critical contributors to the efficient use of leased and owned space by research scientists at MGH. Will identify, categorize, analyze, allocate, and manage space utilized by researchers. Will work with RSMG management and scientists to develop a coordinated approach to the employment of research space. The Space Analyst may serve as a contact regarding space and space-related requirements and as an intermediary between certain groups and various hospital departments responsible for providing research laboratory facilities.Works independently under the general direction of the Supervisory Space Analyst.Meets with Department Directors, Center Directors, Program Directors, Principal Investigators, and other management representatives to investigate past, present, and future program resource utilization (including space, grant dollars, capital equipment and staff) in order to ascertain present and future space-related requirements for research Departments, Centers, Programs, and Cores.The Space Analyst must have sufficient knowledge of how research programs functions to be able to identify inter-program sharing and reallocation of resources so that resource utilization is attributed to the research site where the research actually occurs rather than merely to the administering department. Prepares thorough comprehensive written interim analyses and Final Reports of Research groups resource utilization with particular emphasis on present and future space and space-related needs for review by the Supervisory Space Analyst. The Space Analyst provides an informed scientific and technical perspective during discussions and negotiations with users, architects, and planners regarding the design of options leading to the most efficient utilization of space assigned to research activities. Makes recommendations regarding the use of resources to support activities designed to increase the efficient use of research space. Responsible for representing and protecting the interests of the Research Community during discussions related to utilization of space.Problem solves and makes recommendations regarding the allocation and management of research space. Develops options (based on knowledge of program needs, institutional resources and priorities, and scientific parameters) for utilization of new, alternative, or reassigned research resources.Participates in the ongoing development and utilization of the RSMG Space Management System automated decision-making support system.The Space Analyst is responsible for working with assigned departments in analyzing and planning for new research space needs according to documented increases in funded research. The Analyst, in cooperation with a Senior Space Analyst, will evaluate alternatives to determine if the best location for new research space is within existing hospital sites or requires the construction or lease of new facilities. Prepares written proposals and analyses for new space.The space analyst will develop comprehensive strategic models and set forth plans, based upon financial projections, quality of research, and MGH research mission, to effectively utilize the hospitals research areas.Qualifications:Bachelors level education in field related to biomedical, biological, or medical sciences. Strong scientific backgroundFamiliarity with dynamics and intricacies of research finance mechanisms at an academic facility is helpful.Experience as a member of staff in a research laboratory.

Associates Degree2 Years or more experience required Please note: This position will not be filled until February 2010 JOB TITLE DUTIES & RESPONSIBILITIESRepairs medical equipment to appropriate specificationsProperly documents all work performed on medical equipment.Performs periodic maintenance as part of the Bio-Med PM program.Uses technical knowledge to assist end users with proper operation and care of medical devices. (When Needed) Investigates medical equipment occurrences in a manner consistent with FDA and/or State of Colorado regulations. Uses scientific methods and good investigative techniques to determine root cause of occurrences.Demonstrates versatility by using all skills to benefit organizational operation. Works with other individuals and work groups to solve hospital technical problems.Interacts with clinical staff to assure satisfactory resolution of services calls. Handles service calls in a timely manner. Communicates status and out comes to clinical staff.JOB REQUIREMENTS The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education: 2 years (i.e. Associate Degree) beyond HS Experience: Greater than 2 years License / Certification / Registration ICC certification preferred. Working Environment: Works in a well lit, heated and ventilated area. Position requires considerable mobility throughout the facilities. Potential exposure to routine, communicable diseases through regular contact with employees and the public at large.

Research Nurse Opportunity!

DEPARTMENT: Division of ResearchSCHEDULE: Part-time, 20 hours per week, Evening / Day shift; Monday 4:00pm to 8:00pm, Thursday &Friday 10:00am to 6:00pm or 7:00pm (Occasional Saturday and evenings to phone patients)NOTE: This position is expected to continue for 2 years work or pending continuation of grant/contract funding.EDUCATION/LICENSE/CERTIFICATION: Bachelor´s Degree in Nursing or higher. Current California Registered Nurse license required.JOB SUMMARY: The CHOICES Study is a telephone-based educational intervention to increase patient understanding about clinical trials as a treatment option and increase enrollment in clinical trials. We are currently seeking a bilingual research nurse to join our collaborative study team.QUALIFICATIONS:- Bilingual (English/Spanish) required.- Minimum of two years recent experience as a nurse in an educational environment. Previous research experience and experience in patient education preferred.- Recent experience in oncology preferred- Previous experience in phone counseling preferred.- Must be sensitive to emotional states of newly diagnosed patients- Must be able to make accurate assessments of patient health literacy and tailor educational phone call appropriately.- Experience with Kaiser Permanente data systems highly desirable.- Proficiency in Microsoft Office products (Word, Excel, Access, and PowerPoint) required.- Must demonstrate excellent communication, organizational, and interpersonal skills.- Must be able to work successfully with a wide variety of internal and external project staff and study participants.- Must be able to manage multiple priorities and meet goals under stringent time deadlines.- Must be punctual, detail-oriented, and follow detailed protocols precisely.- Must exhibit a professional manner with a high degree of courtesy, tact, and sensitivity.- Must be able to work independently in a clinical environment with support from the Principal Investigator, Project Manager, Clinic Coordinator, and Assistant Clinic Coordinator.DUTIES: The Nurse Educator is responsible for the implementation of a tailored telephone counseling protocol, documentation, data collection, and evaluation of study research subjects. This involves interviewing, preparing and educating patients for their visit with their oncologist. The Nurse Educator will also complete study follow up activities according to the Protocol. The Nurse Educator screens the medical records of cancer patients to confirm their eligibility to participate in multiple ongoing cooperative group adjuvant clinical trials for various cancers including breast, colon, lung, brain, and lymphoma. Following a tailored telephone counseling protocol, the Nurse Educator will then recruit eligible patients to participate in the CHOICES intervention study. The protocol includes obtaining verbal consent assessing patient understanding about and interest in clinical trials, and providing educational messages tailored according to patient health literacy and language. The Nurse educator will describe the clinical trials process and answer any questions patients may have. The intervention focuses on increasing patient awareness about the opportunity to participate in a clinical trial as a possible treatment option as well as providing needed information and skills to enable patients to have a productive discussion about clinical trials with their oncologist.

Allergan is a global, technology-driven multi-specialty health care company pursuing therapeutic advances to help patients live life to their fullest potential. In making this commitment, we work to develop an unparalleled level of insight into patients wants and needs and into the priorities and concerns of the medical specialists who treat them. To this end, we employ more than 50 percent of our work force in either research and development (R&D) or sales, ensuring our efforts are focused on innovation and our customers.The Opportunity:Provides scientific and technical expertise in experimental and toxicologic pathology within Drug Safety Evaluation. As pathology representative helps design, conduct and interpret in-house and CRO toxicology studies to support Discovery, Pre-Development and Development. Supervises conduct of in-house necropsy and integrates pharmacologic, in-life, organ weight, clinical pathologic toxicokinetic and macroscopic data with microscopic findings in in-house toxicology reports. Peer reviews pathology data for in-house reports. Serves as pathology monitor at CROs, including protocol review, pathology peer review and report review. Implements innovative pathology-based approaches and techniques to solve issues of toxicological concern. Provides investigative pathology support to Discovery Programs. Stays abreast of current literature and trends. Accomplished in working under SOPs in a GLP environment.Provides pathology support for Development projects. Designs and reviews nonclinical protocols based on scientific rationale and/or regulatory guidelines. Supervises conduct of in house necropsy or serves as pathology monitor for CRO studies. Conducts anatomic and clinical pathological and organ weight evaluation and ensures integration of this data with pharmacologic, in-life, toxicokinetic and macroscopic data in discussion/conclusions. Coauthors in house reports and reviews CRO reports with pathology data Conducts pathology peer reviews of in-house and CRO studies. Reviews relevant literature and background information.Provides pathology support for Discovery and/or investigative programs to address target organ toxicity. Participates in designing, reviewing and approving nonclinical protocols. Conducts anatomic pathological evaluation using standard and/or investigative methodology and integrates this data with relevant ancillary data for compound lead selection or investigative evaluation.Represents the Pathology Department on various project/program teams by discussing, contributing to, and reviewing programs, projects and by advising teams and management on timings of completed tasks, important findings and decision making. Participates in review of regulatory and clinical documents regarding nonclinical safety data and human dose setting or risk assessment. Informs management of ongoing and planned project/program activities and potential issues or conflicts. Responds to regulatory or clinical inquiries.Supports departmental objectives by improving existing procedures and practices and introduction of enhanced capabilities. Provides input to staff guidance and training to increase knowledge and skill base. Writes or reviews and revises standard operating procedures and guidelines.Maintains up-to-date knowledge and/or technical advances in the fields of pathology, toxicology, and related disciplines and therapeutic areas, Good Laboratory Practices, and veterinary and laboratory animal science. Benchmarking for industry standards. Cultivation of personal research interests. Contribute to internal and external scientific presentations. Development of productive internal collaborations. Active participation in professional societies.The Requirements:D.V.M.with 6 years postgraduate experience, including Pathology Residency and PhDMinimum of 5 years industry-related experience in toxicologic pathologyBoard Certification by A.C.V.P. or equivalentEstablished research credentialsFamiliarity with current advanced morphologic and other investigative research techniquesExperience with toxicologic pathology of Laboratory AnimalsFamiliarity with spontaneous disease states in Laboratory AnimalsExcellent written and verbal English communication skillsGeneral knowledge and proficiency with Office Automation Software