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12/15/2009 - San Antonio, TX - Healthcare / Facility Administrator - San Antonio ( NW Medical Center - TX )
DaVita
We love our patients. We think you will, too.Make the most of your leadership and management skills to help patients live better lives. As a front-line leader in an outpatient clinic or hospital unit, you will be responsible for all aspects of the centers operation-including superior-quality patient care, physician relations, teammate leadership and financial results. As such, your ability to coach and mentor your clinical team will be critical.If you love patient-centered health care with real relationships inside a company that encourages fun on and off the clock, then DaVita is the place for you.We offer career options to fit your lifestyle.Here is what you can expect when you join our Village as a Facility Administrator.Fun, relationships-based culture-patient- and teammate-drivenFORTUNE 500 stability-with the nations largest independent provider of dialysis servicesTraining Magazine Top 125 award-winning educationMultiple career paths across a variety of cutting-edge modalitiesRewards for your stellar performanceClinical outcomes consistently ranked above the national average-treating more than one-third of the dialysis population (thats approximately 100,000 patients!)Exceptional benefits-including the healthcare industrys most generous profit sharing programDedication above all to caring for patients suffering from chronic kidney failure-at over 800 hospital units and approximately 1,300 outpatient dialysis clinics nationwide
Posted on iHireHealthCareAdministration.com
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7/30/2009 - Titusville, NJ - Clinical Research Physician Scientists/CNS (Associate Director Project Physician level
Johnson & Johnson
Johnson and Johnson Pharmaceutical Research and Development, L.L.C., a member of Johnson and Johnsons Family of Companies, is proactivelyseeking qualified candidatesfor futureClinical Research Physician Scientists/CNS positions, to belocated in Titusville, NJ.Johnson Johnson Pharmaceutical Research Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.In this role, the candidate will be a responsible member of a clinical team dedicated to the development and execution of medical strategies and the clinical and operational implementation of a complex compound program. The candidate provides active medical and scientific contribution to a cross-functional clinical team developing a new molecular entity currently being studied for central nervous system applications. Team matrix interactions include project planning, project direction, regulatory affairs, data management, medical writing, biostatistics, worldwide medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business related disciplines. The candidatemay be asked to contribute to the evaluation of scientific opportunities in the CNS area.The role requires a high-performing, and high-energy individual who demonstrates outstanding scientific and technical leadership, influence, the highest personal and ethical standards, and exceptional oral and written communication skills.Responsibilities and Expectations, in concert with staff, include: Responsible for medical monitoring/reporting and company safety officer activities; Evaluates adverse events (pre and post-marketing) for relationship to treatment; Assists Regulatory Affairs in determining requirement for any corrective actions or health authority reporting; May act as a medical contact at the company for the Food and Drug Administration and other worldwide health authorities concerning clinical/medical issues; Interprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for FDA submissions; Assists Regulatory Affairs in the development of drug/device regulatory strategies; May act, in concert with senior clinical personnel, as a company spokesperson regarding publication of clinical research findings and presentations to relevant FDA advisory committees; Helps explore and evaluate new product ideas to assist in identifying new marketing opportunities; Support general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance; Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.Additionalresponsibilities include:Reviews medical literature and related new technologies; May be asked to assess external clinical research proposals involving company products relevant to companys mission; May be asked to assess medical publications emerging from the Team and its affiliates;May be responsible, with appropriate colleagues, for review of Company advertising and promotion; Acts, in concert with medical staff, as a liaison between company and clinical investigators; Develops, in concert with senior clinical staff, credible relationships with opinion leaders, medical directors, and key regulatory officials.
Posted on iHirePhysicians.com
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11/19/2009 - Rockland, MA - Medical Director, Oncology
Merck Serono
EMD Serono, Inc. (the US affiliate of Merck Serono Merck KGaA) is expanding its US Oncology unit. As part of this effort, we are seeking an individual to fill a key role in the development and direction of its new Oncology Medical Services (Medical Affairs) group, based in Rockland, Massachusetts just 20 miles Southeast of Boston.EMD Serono Oncology is focused on developing novel, first-in-class, targeted cancer therapies that provide beneficial therapeutic outcomes and create new therapy options for cancer patients. The development of these targeted cancer therapies is based on the targeting of three therapeutic platforms: the tumor cell, the tumor environment, and the immune system. Merck Serono markets Erbitux (Cetuximab) ex-US. In addition, EMD Serono Oncology has more than 10 pipeline products with many currently in phase I-III clinical trials. Foremost among these pipeline agents are Stimuvax, a therapeutic cancer vaccine, and Cilengitide an anti-angiogenic integrin inhibitor, both in phase III studies. Additional pipeline agents include an antibody integrin inhibitor, therapeutic cancer vaccines, immunocytokines, a TLR9 immunomodulator, and inhibitors of MEK, aurora kinase inhibitor, and c-MET.Under the guidance of the Vice President of Oncology Medical Services, this new role will offer the incumbent an exciting opportunity to develop and direct an emerging function within the US organization. This opportunity includes the initiation of medical strategy and the development of partnerships with key US organizations. The Medical Director will play a key role in establishing relationships with the NCI, US cooperative groups, and US investigators in the development and oversight of clinical research studies. This individual will also serve as a prominent representative of Medical Services in cross-functional teams within the Oncology unit.Key Responsibilities:Establishes partnering relationships with key members of the NCI and US cooperative groups and key US investigators and thought leadersAssists in the development and provides oversight of clinical research studies with the NCI, US cooperative groups, and US investigatorsParticipates in relevant Global Product Teams to ensure alignment of US Medical Sciences with global clinical development and life cycle plansAids in the design and implementation of Medical Sciences programs for current pipeline and future approved productsEnsures the appropriate scientific and medical content of Medical Sciences programsEvaluates Independent Medical Grants (i.e. Investigator Sponsor Trials) in collaboration with IMG teamRepresent Medical Sciences in providing scientific and clinical expertise at medical meetings, advisory boards, and outreach meetings at key US institutionsInteracts with other cross-functional units, including Clinical Development, Regulatory, Medical Operation, Safety, Medical Information, Marketing, etc. on cross-functional projects to ensure cross-functional alignmentMedical representative on the internal Promotional and Scientific Materials Review (PSMR) committeeCollaborates with sponsors and/or internal departments on the review of study-related abstracts, posters and publicationsOffers medical leadership regarding CME grantsProvides awareness on clinical and drug development information relevant to responsible programs by review of literature, attendance at medical/scientific meetings, and personal interchanges with consultants and investigatorsAssists the VP in the future development, hiring, direction, and job enrichment of MSL, Medical Communications, Publications, and IST Operations teams
Posted on iHireHealthCareAdministration.com
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12/29/2009 - Alexandria, VA - MEDICAL RECORDS CLERK III
Inova Health System
Demonstrated knowledge of computer systems used in Health Information Management Department. Demonstrates attention to detail in daily functions. Requirements: One-year medical record filing experience. Seeking someone with: transcription experience, medical terminology training, revenue cycle support experience, quality/audit review experience, and corrections experience. Education Requirements: High School Diploma or equivalent.
Posted on iHireMedicalSecretaries.com
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1/13/2010 - Belleville, NJ - Dietary Aide (TP)
Saint Barnabas Health Care System
Reheats and serves food trays to patients. Stocks service areas, prepares and serves snacks and performs other general duties. Assists in the distribution, collection and preparation of patient menus. Performs a variety of routine kitchen duties as assigned. High school graduate or equivalent.Prior work experience in a hospitality environment highly preferred.
Posted on iHireNutrition.com
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1/22/2010 - Long Branch, NJ - Adjunctive Therapist Behavioral Health STCF Per Diem
Saint Barnabas Health Care System
The Adjunctive Therapist provides individual and group therapy through the use of non-verbal media and verbal expressions. The Adjunctive Therapist utilizes the creative processes in his/her area of expertise (art, movement, dance music, recreation), to elicit non-verbal communication and expression. Range of services include, but are not limited to: Preventive services, diagnostic evaluation, assessment and treatment using creative arts therapy techniques and process. Translates the treatment goals of the interdisciplinary team into creative arts methodology.Requirements:Education/Training/Certification/Licensure:A minimum of a BA/BS with national certification in their specialty is required. MA/MS preferred. Area of Concentration: Non-verbal group therapy modalities.One to three years creative arts therapy, clinical internships and/or certification by approved credentialing agencies/associations.Psychiatric inpatient experience preferred.
Posted on iHireMentalHealth.com
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1/13/2010 - Belleville, NJ - Dietitian (TP)
Saint Barnabas Health Care System
Provides medical nutrition therapy to patients in the acute care and/or rehabilitation setting. Participates as a team member in performance improvement, education and administrative activities needed to support the Food and Nutrition Services Department. Expertly completes nutrition screening, assessment and care planning. Provides continuity in care with an emphasis on beneficial outcomes to the patient. BS degree in nutrition-related field. Registered Dietitian accredited with the Commission for Dietetic Registration (CDR) or RD Eligible. One year experiencepreferred in clinical nutrition.
Posted on iHireNutrition.com
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1/13/2010 - Bar Harbor, ME - Animal Care Trainee I (2010) (2240)
The Jackson Laboratory
2240 Job Description The Jackson Laboratory has current career opportunities within Animal Care. Successful candidates will undergo extensive training including classroom and on-the-job training to learn all aspects of animal husbandry such as feeding, watering, sanitation, monitoring both animal health and environmental parameters as well as mouse colony management. Colony management includes setting up new breeding units, tracking breeder performance, weaning and preparing mice for shipment along with other husbandry duties. Required Skills Successful applicants must have a minimum of HS diploma or GED and prior work experience. Individuals with two-or four-year degrees in Animal or Life Sciences have the opportunity to advance more quickly along the various program career tracts. Job Location Bar Harbor, ME, US. Position Type Full-Time/Regular
Posted on iHireVeterinary.com
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8/10/2009 - San Juan, - Clinical Innovations|Clinical Advisor-RN|Puerto RicoCL91LE
Humana
Humana Inc., headquartered in Louisville, Kentucky, is one of the nation's largest publicly traded health benefits companies. Humana offers a diversified portfolio of health insurance products and related services - through traditional and consumer-choice plans - to employer groups, government-sponsored plans, and individuals. Today, Humana is a leader in consumer engagement. Throughout its diversified customer portfolio, the company provides guidance that can both help lower costs and lead to a better health plan experience.
Posted on iHireNursing.com
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10/2/2009 - Salem, NJ - Social Worker - Hospice - Per diem
Community Health Systems
The Medical Social Worker shall be responsible for assessing, planning, evaluating and implementing a plan of care based on the psychosocial needs for Home Health Care and Home Health Hospice Care clients to promote their optimal social functioning; participates in Hospice Bereavement Program; participates in and manages the Volunteer Program. Medical Social Services will be provided in accordance with agency policies and procedures, applicable health care standards, and governmental laws and regulations.
Posted on iHireSocialServices.com
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