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MMC serves as a community hospital for the people of greater Portland, Maine and as the premier tertiary care center for northern New England

Summary of Position DescriptionThe Research Nurse Coordinator position involves many aspects of research coordination with the Division of Nursing. The incumbent reports to and collaborates with the Director Center of Nursing Research and Quality Outcomes, the Principle Investigator, and relevant MMC Departments. The primary responsibilities include study coordination and acting as a hospital educator/resource person for studies.The Research Nurse Coordinator, - conducts all research activities within an ethically based framework and in accordance with good clinical practice. - develops and/or evaluates new research protocols/proposals with investigator(s) considering feasibility of conduct as the site. - collaborates with other departments and disciplines to plan and implement relevant aspects of the protocol/proposal. - maintains ongoing communication with IRB throughout all phases of the study/studies; participates in informed consent process.- facilitates timely completion of grant proposal. - coordinates ongoing conduct of study through to completion. - coordinates research, quality and evidence based practice education.- coordinates staff presentations at professional meetings/conferences. This includes overseeing poster development, and writing/reviewing abstracts and manuscripts as appropriate.- collaborate in the development of research related data collection methods and analysis; this includes, for example, designing case report forms, and associated databases.Minimum Knowledge, Skills, and Abilities Required1. Current license to practice as a Registered Nurse in the State of Maine.2. Knowledge of current research related policies and procedures as well as appropriate process for initiating revisions.3. Thorough knowledge of theory, practice, principles, processes and issues of nursing usually acquired through 2-3 years of clinical experience.4. Analytical ability necessary to keep records, maintain inventory levels and perform data entry.5. Ability to manage complex projects through all phases of development, implementation, and follow-up.Department: Nursing Offices Schedule: Full Time Shift: First Shift (Day) Hours: 40

Who Cares? We Do!For our patients, our communities, and each other Allina Hospitals & Clinics!Located in Minnesota and western Wisconsin, we are a not-for-profit system of hospitals, clinics and other health care services, united in caring for our patients with unparalleled talent, knowledge and technology; caring for our communities through collaborative efforts to promote stewardship, compassion and wellness; and caring for each other in an environment that puts patients first and helps passionate people excel. This is what makes Allina unique. Won’t you join us?Abbott Northwestern Hospital is the largest not-for-profit hospital in the Twin Cities with a longstanding tradition of compassionate care and service; centers of excellence in cardiovascular care, oncology, neuroscience, orthopedics and obstetrics; and leadership in education and clinical research. Located in Minneapolis, Minn., Abbott Northwestern is a 633-bed hospital. Its 5,330 employees and 1,586 physicians care for nearly 370,000 patients and their families each year from the Twin Cities area and throughout the Upper Midwest.Responsibilities:Project Manager is responsible for managing conduct of oncology research trials. Will work directly with researchers to develop research projects, seek grant funding and oversee all aspects of the trial conduct. Will ensure all staff is adequately trained and provide ongoing oversight / mentorship to ensure competence in the conduct of research and compliance with all agencies governing research. He / she will coordinate large projects within VPCI research department as well as collaborate with other departments and systems in the hospital that see oncology patients. Collaborate with external researchers. Assists in development and implementation of department databases / information systems that effect the operation of the research department. May provide clinic coverage.Qualifications:- BS degree in biological sciences. RN or relevant clinical background highly preferred. - 4-6 year´s previous clinical research experience required. - 1-2 year´s previous management experience preferred. - Previous experience in research project development and management in an oncology setting ideal. - ACRP CRC desired. Able to work independently and interdependently in multidisciplinary team environment. Needs to have knowledge and understanding of all aspects of research including design, development, and project management ensuring compliance with all regulatory agencies governing research and protection of human subjects. Ability to obtain knowledge of new advances in research and implement into department procedures. Strong interpersonal, communication, and people skills required. Individuals in this position should be able to proactively manage internal and external researcher / research organization expectation. Develop project schedules, and facilitate projects coming in on time and within budget. Strong attention to details. Strong computer skills including Microsoft office products.- Pay, Benefits & Work Schedule:- 40 hours per week; Monday - Friday - Day shiftsAllina is proud to offer highly competitive salaries and comprehensive benefits that include a 401(k)/403(b), tuition reimbursement, day care reimbursement accounts, banking services and much, much more. Check online for other opportunities throughout Allina! We have a place for you at Allina Hospitals & Clinics.

Serve as a member of a close-knit research team conducting inpatient and outpatient clinical trials investigating the efficacy of combining pharmacotherapies and behavioral interventions for the treatment of opioid, cocaine, and tobacco addiction.

General Purpose: * Serve as a member of a close-knit research team conducting inpatient and outpatient clinical trials investigating the efficacy of combining pharmacotherapies and behavioral interventions for the treatment of opioid, cocaine, and tobacco addiction. * Under the supervision of the Principle Investigator (PI) and with substantial use of discretion and independent professional judgment, provide services to clients in treatment research studies. These studies will be conducted at the West Haven VA Hospital. * Exercise discretion and independent judgment in performance of job duties.Position Description: - Dispense medication, supervise control of medication and administer medication for clients enrolled in research protocols.- Perform history physical examinations. - Provide research nursing support across a variety of studies, both inpatient and outpatient. This may include the taking of vitals, ordering blood and urine toxicology, the monitoring of patients during drug administration studies, and the accurate collection of relevant nursing data. - Review diagnostic tests (e.g. blood work, EKGs, and blood pressure) to help assess clients. - Participate in clinical, diagnostic, and evaluatory conferences, providing preliminary or follow-up data. Document patient´s symptoms and follow-up in timely manner.- Schedule clients for clinical and laboratory procedures.- Compile weekly dispensing materials for pharmacist and physician. Develop a weekly medication-dispensing roster. Perform data entry on missed medication, dose changes, etc.- Ensure that nursing and clinical records are current and are maintained according to state and federal guidelines as well as guidelines of the research protocol.- Provide direct client services, including administration of study medications and research instruments. - Attend weekly research and supervision meetings. May participate in such activities as orientation and training for research assistants or other research staff. Attend appropriate clinical meetings, seminars and in-service training programs.- Responsible for the protection of patients rights and confidentiality, as prescribed by funding, regulatory, and treatment program policies.- May serve as backup for other research and staff nurses to cover vacation, sick time, etc. This may include early morning hours.- May be asked to serve as part of a regular Saturday rotation for dispensing medications.- Perform other related duties as required.Qualifications: - Bachelor of Science in Nursing and six years of related experience; or an equivalent combination of education and experience.- APRN or PA licensure in the State of Connecticut.- At least one year of related experience, particularly in the area of mental health nursing.- Must successfully complete the VA credentialing.- Preferred: Previous experience working with substance abusing individuals and the dispensing of Methadone.Yale University offers exciting opportunities for achievement and growth in New Haven, Connecticut. Conveniently located between Boston and New York, New Haven is the creative capital of Connecticut with cultural resources that include three major museums, a critically-acclaimed repertory theater, state-of-the-art concert hall, and world-renowned schools of Architecture, Art, Drama, and Music.We invite you to discover the excitement, diversity, rewards and excellence of a career at Yale University. One of the country´s great workplaces, Yale University offers exciting opportunities for meaningful accomplishment and true growth. Our benefits package is among the best anywhere, with a wide variety of insurance choices, liberal paid time off, fantastic family and educational benefits, a variety of retirement benefits, extensive recreational facilities, and much more.Yale University is an affirmative action/equal opportunity employer. Yale values diversity in its faculty, staff, and students and strongly encourages applications from women and members of underrepresented minority groups.

The Department of Clinical Trials within The Methodist Research Institute located in the Texas Medical Center, Houston, Texas, seeks a full-time Clinical Research Nurse.The Clinical Research Nurse coordinates complex research projects that may involve sites and/or the supervision of research activities; implements research protocols, including screening and enrolling subjects, obtaining blood and other specimens for tests and cultures, administering medications and maintaining pertinent patient records. He/she will work with Principal Investigators and team of researchers and demonstrate knowledge of nursing with clinical skills and theoretical knowledge necessary to manage care of high acuity patients. The candidate will obtain, record, validate, and interpret data to achieve the goals of the research project; conduct studies according to protocol and complete case report forms. Clinical Research Nurse applicants educate patients in significant aspects of study, ensures that clinical studies are conducted in accordance with FDA guidelines and other regulatory agencies. The person serve as liaison between physicians, patients, staff and sponsors; may assist in developing the clinical trial agreement, and may provide guidance and work direction to entry level research nurses.REQUIREMENTS: Graduate of an accredited school of professional nursing with a current Texas license. Preferred is, (1) a Bachelor of Science in Nursing or an equivalent combination of relevant education and/or experience, and (2) a research certification.

Full time research nurse needed to join busy, multi-site ortho/pain management practice

Full time research nurse needed to join busy, multi-site orthopedic and pain management group. Two years relevant research experience required

Assists with providing organization and support to the research functions of Graduate Medical Education and other hospital departments as needed. Participates in complex clinical trial duties with assistance as needed. Has knowledge of the clinical trial process and the regulations governing it. Performs data management and assists with interpretation specific to clinical trials through appropriate Carilion-affiliated research groups and institutions. These activities include Institutional Review Board (IRB) approvals, registration, compilation, and submission of data and the monitoring of quality of care and study compliance. Maintains a system for perpetuation of effective data flow.Assists with coordinating various disciplines and functional areas as they relate to each specific trial. Collects, submits and maintains appropriate patient data and regulatory documents. Communicates data to appropriate resources in an effective and efficient manner.Utilizes knowledge and attention to detail to execute all data management activities. Maintains a system for organizing, planning and coordinating the work flow related to IRB approval and patient accruals to clinical trials, including development of appropriate consent forms, patient and family education and communication regarding adverse drug reactions. Serves as a patient resource, creating patient teaching plans and educating patients and family members.Assists in maintaining a quality control program as mandated by the study groups and Carilion Clinic. Assists with the evaluation of the quality of patient care and compliance to protocol requirements. Uses problem solving skills to identify opportunities for improvement and completes projects in a timely and effective manner. Uses exceptional communication skills as a liaison between institutional investigators, IRB, the affiliated study groups? Office of Sponsored Programs and study sponsors. Coordinates and assists with the maintenance of investigational drug records.Maintains a system of effective communications among physicians and staff regarding the availability of clinical trials for patient accrual and eligibility requirements. Responsible to work with principal investigator to achieve a target number of accruals.MINIMUM QUALIFICATIONS:Education: Bachelor´s degree in biology or medical/clinical sciences (i.e. physiology, nursing, etc.), or a related field. Graduation from an accredited nursing program required.Experience: One year of Clinical Research experience preferred.Licensure, Certification or Registration: License or certification specific to the discipline according to Virginia requirements. Current license to practice as a Registered Nurse.Other: Thorough knowledge of medical terminology and human anatomy and physiology. Working knowledge of the disease/condition under study, the clinical trial process and good clinical practices. Proficient in the application of federal regulations and the Good Clinical Practices governing clinical research. Must be competent in word processing and spreadsheets. Proficient with data base management systems and statistical software, research methodology, and statistical analysis. Must have effective interpersonal and problem-solving skills. Must be self-directed and excel in attention to detail. Must use good judgment with regard to priorities and deadlines.Service Excellence and Quality are hallmarks of Carilion Clinic. As a team member, you will be expected to consistently deliver the best in care and customer service. As an employee, you will demonstrate respect, dignity, kindness and empathy in each encounter with our patients, families, visitors and with each other.Carilion Clinic is an Equal Employment Opportunity/Affirmative Action Employer.

Recognized nationwide for delivering innovative, leading-edge patient care, Cedars-Sinai is an independent, not-for-profit, academic health system. Cedars-Sinai offers a dynamic patient care, research and teaching and community service environment.

Job Category: NursingJob Specialty: ResearchPosition Type: Regular-F/TShift Length: 8hrHours: 8:00 a.m. - 5:00 p.m. Days: Monday - FridayShift Type: DayWeekends: As Needed Job Description: RESEARCH PROGRAM COORDINATOR/RESEARCH NURSECedars-Sinai Medical Center is both a leading research institution and a world-class educational facility for tomorrows physicians and scientists. After years of individual and joint research, two of our eminent physician scientists Stephan Targan and Jerome Rotter have developed Combinatorial Genomics, a new platform technology that, by melding genomics with biologic pathway identification, enables coordinated target discovery allowing for identification of diagnostics and therapeutics. Its name is Tarrot.As a business unit of Cedars-Sinai, Tarrot offers a unique value proposition, which focuses the company on emerging trends, opportunities and scientific discovery in the rapidly changing Life Science market. Tarrot currently has an opportunity available for a Research Program Coordinator/Research Nurse. RESPONSIBILITIESThe Research Program Coordinator/Research Nurse coordinates all aspects of implementation of research for the Principal Investigator including, but not limited to recruitment, documentation, submission or IRB materials, interface with sponsor/clinical research, compliance with all federal and local requirements, protection of patient safety, and provision of technical support related to data collection. Be able to provide technical nursing support related to data collection of research protocols, including tissue sample collections (phlebotomy, pathological tissues, etc.), processing (spinning, triaging, DNA isolation, pellet formation, etc.) and data collection reporting to principal investigators and/or pharmaceutical company representatives. Will act as administrative coordinator for multi-study projects and is responsible for day to day operations of projects, including oversight of patient recruitment, financial and statistical analysis, and data collection. Will participate in conceptualization and design of future projects and work with the data management team to provide technical assistance on data compliance with regulatory guidelines. Education and Work Experience Preferences: EDUCATION and/or EXPERIENCE:Current California RN Licensure with three to five (3 5) years experience coordinating clinical research studies and clinical trials. Two (2) years experience in data management, including design and maintenance of databases. Strong interpersonal skills to work effectively with patients, physicians, families, pharmaceutical companies, and other project personnel. Must demonstrate excellent communication skills, written and verbal.

Job Specialty: ResearchPosition Type: Regular-F/TShift Length: 8hrHours: 8am - 4:30pm Days: Monday - FridayShift Type: DayWeekends: None Job Description: Cedars-Sinai Health System, Neurology Department has an opening for a Research Nurse to work under general supervision and coordinates all aspects of research in the Neuro Oncology Center, including interactions with research personnel and project participants, data related tasks, patient recruitment, patient education, clinical patient assessment / reassessment / follow-up activities and logistical organization.The Research Nurse will also write and submit IRB applications and budgets for new studies in Neuro Oncology,ensure appropriate documentation and compliance with clinical trials, maintain records for site review and grant/study submission, organize data collection, including SAE and AE forms, etc., serve as a liaison between the study participants and PI and/or other research staff, prepare data spreadsheets for Investigator and/or Department, prepare and updates investigation binder and complete CRFs and may assist in training of other staff members. Education and Work Experience Preferences: Educational Requirements:Master´s preferred; BSN requiredLicense/Certification/Registration Requirements:Valid California Registered Nurse license, and current BLS (Basic Life Saving Certificate)Experience:• Prior experience as a clinical research nurse preferred with working knowledge of FDA and IRB protocols. Experience with Neurosurgical/Neurology pts. preferred.• Excellent verbal and written communication skills required.Physical Demands:Must be able to safely lift 35 lbs; prolonged sitting

Hebrew SeniorLife (HSL) is a 100+-year-old organization dedicated to providing seniors with the highest quality of life through an integrated network of health care, research, housing and teaching programs in the Greater Boston area.

It is the largest nonprofit provider of senior health care and housing in New England. Our mission is to honor our elders by respecting and promoting their independence, spiritual vigor, dignity and choice and by recognizing that they are a resource to be cherished. Our health-care network comprises Hebrew Rehabilitation Center, a long-term, sub-acute, and long-term medical acute care facility in Boston; three senior housing sites-Jack Satter House in Revere, Simon C. Fireman Community in Randolph, and Center Communities of Brookline; and Orchard Cove, a life-care community in Canton. The Institute for Aging Research in Boston, affiliated with Harvard Medical School, is one of the most prestigious aging research facilities in the country. HSLs NewBridge on the Charles, our premier multigenerational continuing care retirement community in Dedham, consists of 256 independent living units, 50 assisted living units, 41 memory support assisted living units, and a 268-bed Health Care Center, which offers long-term and sub-acute care. Hebrew SeniorLife also offers services to the community, including Adult Day Health programs and outpatient clinics in audiology, exercise, memory disorders, osteoporosis screening, and rehabilitation.The Aging Brain Center, part of the Institute for Aging Research, currently has an exciting opportunity for a Research Nurse. This would be a great fit for someone with strong leadership skills and who is highly self-motivated. In this role, your main responsibility will be recruiting and conducting interviews with elderly patients for a large multi-project, multi-site study, including cognitive assessments, neuropsychological testing, and medical record review. You may have administrative coverage responsibilities including oversight and management of research assistants, trainees, and other staff. You will also provide for the safety of elderly research participants throughout research interactions and visits; assess participants for fatigue and adverse events, and report participant hazards and adverse events to Project Director.Qualifications: - BSN required, with at least 2-3 years of prior research experience, and at least 2-3 years of nursing experience. - You must be experienced in clinical epidemiologic interviews and medical record abstraction. Phlebotomy experience preferred. - You must be able to manage the special needs of a frail senior population, for example: assessing and addressing fatigue and assessing and providing for comfort during study procedures. - You must also have computer skills, MS Word, Internet and Email; familiarity with Excel and MS Access are preferable. - Excellent communication (both oral and written) and interviewing skills are essential. - You should also have working knowledge of the regulations governing the conduct of human studies research. - Previous experience working with seniors, and conducting physical cognitive assessments, are preferred. - You will also need to provide your own transportation to and from patients homes.Hebrew SeniorLife (HSL) is an equal opportunity employer, and we offer a competitive compensation and comprehensive benefit package, as well as many opportunities for personal and professional growth. If you are motivated by new opportunities and seek a stimulating and rewarding career, we invite you to join our diverse team of talented professionals who are dedicated to helping seniors and their families. Everything we do flows from these tenets and are further inspired by the duty of tikkun olam-to heal the world.To learn more about Hebrew SeniorLife and our career opportunities, visit our Web site at www.hebrewseniorlife.org

As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide.This position is responsible for managing in-depth complaint investigations, with expert product knowledge. This role is responsible for report submissions to regulatory bodies and providing information to Baxter business units for decision-making purposes. This position is a subject matter expert in the team and will train and mentor other Product Surveillance Quality Associates.- Process high-risk (Death/Serious Injury) complaints without supervision.- Determine report ability of a complaint and submit associated Medwatch reports within 30 days per regulations.- Lead the investigation, including developing investigation plan, defining members of investigation team and their roles and responsibilities, plan on-site visits, follow-up communication with internal and external customers.Job Requirements- Expert knowledge of the FDA Quality System and Medical Device Reporting regulations (21 CFR 803, 806, 820 and 211.) Understanding of regulations governing markets outside the U.S.- Expert understanding of the product’s intended use and manufacturing process of assigned products. Ability to prioritize multiple high risk projects to ensure compliance with regulations and standard operating procedures. Excellent problem solving and analytical skills.- Bachelor’s degree in Nursing or Medical Technology is required. 7 years experience, which should include Product Surveillance, direct clinical/medical experience, or relevant product/technical expertise. Experience managing CAPA is preferred.- Travel to customer sites to obtain information pertinent to the investigation, including sample, clinical and engineering information- Guide Specialists leading high-risk investigations, review Medical Device Reports associated with death and serious injury.- Produce and maintain annual base line reports, Alternative Summary Reports and 24-Month Reports as required by the Medical Device Reporting regulation- Perform trend reporting and escalate results to appropriate business units for consideration of necessary actions.- Represent Product Surveillance on Product Improvement Teams, as well as CAPA.Baxter provides its employees with comprehensive compensation and benefits. To view other opportunities at Baxter and to learn more about the company, please visit our Web site at http://www.baxter.com/about_baxter/careers EOE M/F/D/V.