Friday, January 31, 2020

University of Washington Multiple Sclerosis Research/Neurology

The University of Washington Department of Rehabilitation Medicine is an academic and clinical department in the School of Medicine and Affiliated Hospitals which includes the UW Medical Center, Harborview Medical Center, Seattle Children’s, Northwest Hospital & Medical Center, Valley Medical Center, and the VA Puget Sound. The Department offers four degree programs including entry-level degrees in Occupational Therapy, Physical Therapy, and Prosthetics & Orthotics and a PhD in Rehabilitation Science. There are also extensive research programs within the Department with over $13 million in grants per year.

The Department of Rehabilitation Medicine is home to one of the nation’s leading multiple sclerosis (MS) rehabilitation research programs, which is excited to offer an outstanding opportunity for a Research Study Assistant (100% FTE). This individual will join the research team at the UW Multiple Sclerosis Center, a comprehensive multidisciplinary specialty center that serves patients with MS throughout the Pacific Northwest. Current studies focus primarily on enhancing quality of life, improving psychological coping, and managing MS-related symptoms, including fatigue and chronic pain. Several of the clinical trials are evaluating innovative telehealth interventions.

We are seeking a highly motivated, interpersonally skilled, inquisitive, and organized individual to assist with the day-to-day administration of our research program focused on improving the lives of people with MS. This is a great opportunity to obtain valuable experience as a coordinator responsible for the daily operations of research studies involving human subjects. As described in greater detail below, responsibilities will include study-specific tasks related to the day-to-day administration of these studies under the direction of a research manager and Drs. Dawn Ehde and Kevin Alschuler, and in conjunction with a team that includes additional faculty (including physicians and psychologists), research staff, postdoctoral fellows, graduate students, and volunteers. The research study assistant will also have the opportunity to support team activities related to program management under the direction of the research manager.

Duties:

Subject Recruitment and Enrollment:
Field telephone calls from individuals who have seen recruitment materials for the study and are interested in participating. Approach individuals via mail, telephone and in-person during appointments to see if they would be interested in participating. Screen subjects for eligibility using an approved recruitment script. Verify study eligibility via medical record review as part of the screening process. Answer any questions individuals have about the research study. Obtain informed consent from prospective subjects over the telephone and in person. Ensure proper tracking of the overall outcomes of subject recruitment and enrollment.

Conducting Study Assessments:
Schedule, track, and conduct study assessments over the telephone and in-person with enrolled subjects. Administer neuropsychological tests to subjects. Maintain confidentiality of subject records.

Medical Abstraction:
Extract technical, medical, and/or behavioral information from institution or clinical records of research subjects. Screen medical records for study eligibility.

Data Entry, Maintenance, and Monitoring:
Enter data from telephone and in-person assessments into a Microsoft Access and/or REDCap database according to project protocol. Track rate of assessments completed. Use statistical and database management programs to analyze data and prepare summary narrative reports, graphics, tables, and charts.

Database Maintenance:
Maintain components of Microsoft Access and REDCap databases.

Subject Contact:
Act as one of the primary contacts for subject inquiries regarding study protocol. Contact subjects regarding missing data. Send and track payments of subjects when applicable.

Other:
Perform related duties as needed, including similar work on other research studies. Other duties may include copying, filing, data entry, updating procedures, attending and reporting at team meetings, etc.

Minimum Requirements:
Two years of college level course work in a relevant academic area AND one year of experience or equivalent education/experience.

Additional Requirements:
  • Excellent organizational, interpersonal, and writing skills.
  • Experience recruiting, screening, and enrolling subjects via telephone and in person.
  • Experience conducting research interviews or assessments with subjects via telephone around issues related to patient reported outcomes.
  • Proficiency in using Microsoft Office, including Access.

    Desired:
  • Bachelor’s degree in psychology or a relevant academic area.
  • Experience working with people with disabilities.
  • Experience using REDCap and other data management systems.
  • Familiarity working with ORCA and/or EPIC applications.
  • Completion of at least one course in research methods and/or statistics in a social sciences field.
  • At least one year’s experience working on a research study examining health issues, or relevant education/experience.

    This position will work with clinical research involving human subjects within UW Medicine and therefore clinical RSC training is required. The training requirement for this position includes UW Medicine-specific as well as general training.

    The successful candidate will work during normal business hours (8am-5pm) Monday through Friday, but may be asked occasionally to complete telephone interviews in the evening and weekends to accommodate certain subjects’ schedules.

    Application Process:
    The application process for UW positions may include completion of a variety of online assessments to obtain additional information that will be used in the evaluation process. These assessments may include Work Authorization, Cover Letter and/or others. Any assessments that you need to complete will appear on your screen as soon as you select “Apply to this position”. Once you begin an assessment, it must be completed at that time; if you do not complete the assessment you will be prompted to do so the next time you access your “My Jobs” page. If you select to take it later, it will appear on your "My Jobs" page to take when you are ready. Please note that your application will not be reviewed, and you will not be considered for this position until all required assessments have been completed.

  • Committed to attracting and retaining a diverse staff, the University of Washington will honor your experiences, perspectives and unique identity. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable and welcoming.
    The University of Washington is a leader in environmental stewardship & sustainability, and committed to becoming climate neutral.
    The University of Washington is an equal opportunity, affirmative action employer. To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 / 206-543-6452 (tty) or dso@uw.edu.

    APPLY 

    Wednesday, January 29, 2020

    Cardiology Clinical Research Florida

    Are you ready to do more with your career? Established cardiology practice site seeking an experienced Clinical Research Coordinator (CRC) to work in our Research Office.
    Position involves coordinating cardiology clinical trials, including, subject recruitment and enrollment, conducting patient visits, performing protocol procedures, recording adverse events, and performing data entry.
    You will be working as part of an experienced clinical research team. The office and physicians have a national and international reputation for excellence in cardiology, and for the conduct of cutting edge clinical research.
    Responsibilities:
    • Assist in screening, scheduling, and enrolling subjects and with recruitment and community outreach efforts.
    • Conduct study visits, including performance of vital signs, ECG, blood draw and processing.
    • Serve as study resource for patients and family.
    • Distribution and accounting for investigational drugs.
    • Assist with regulatory binders and QA/QC Procedures
    • Maintain quality documentation for all aspects of the study including records and databases.
    • Other duties as assigned or required by the study protocol.
    Skills/Qualifications:
    • Clinical Research Coordinator- Minimum 2-3 years of experience.
    • CCRC or CCRP certification (or eligible) preferred.
    • Patient care experience as a licensed health professional.
    • Good interpersonal and organization skills.
    • Self-directed, proactive with careful attention to detail., thorough and timely in the management of responsibilities.
    • Ability to work independently and on a team.
    • Ability to demonstrate respect and professionalism for subject’s rights and individual needs
    Please reply by email, and attach your resume/CV. Please also include your desired salary and potential start date. Emails without these items cannot be considered.

    Naples Florida (239) 261-2000

    Thursday, January 2, 2020

    Johns Hopkins OB/GYN Clinical Research Coordinator

    Research Coordinator
    Project:
    Women reproductive research.
    General Overview:
    As we are expanding with additional projects, our research team is looking for an excellent self-motivated, goal-oriented, organized, team player Research Coordinator. She will be hired for a Full-Time Position in the Reproductive Sciences and Women’s Health Research division of the Department of Gynecology and Obstetrics; Monday – Friday 8 am-5 pm. The Principle Investigator of the project is Dr. Mostafa Borahay. Current project focuses on uterine fibroid research. The range of duties includes, but not limited to, Institutional Review Board (IRB) applications, patient recruitment, scheduling and conducting study visits, obtaining informed consent, data entry, and records management, expenditure oversight, collecting and processing bio-specimens, communicating with team members on the status of project. Candidate is expected to take ownership of her work and be a trouble shooter. Effective communication and interpersonal skills are critical as the position involves significant interaction with patients.
    Job Duties:
    • Will be involved in the research program including clinical trials in compliance with institutional and federal regulations.
    • Get involved with the start-up phase through to the completion phase of the clinical trial.
    • Will be involved in regulatory application, protocol implementation, compliance, recruitment, retention, and final completion of the trial.
    • Complies with all regulatory/IRB guidelines including, but not limited to: preparation and submission of study protocols, consent forms, amendments, and annual continuing reviews.
    • As such, will collaborate in development, preparation, and maintenance of regulatory documents; collaborate in determination of roles and responsibilities of study team members in the implementation of assigned clinical trials.
    • Collaborate in the development of study tools including data collection forms, eligibility checklists, and pre-printed orders.
    • Prepare and submit Institutional Review Board (IRB) applications, both new and renewal.
    • Follow all institutional research rules and guidelines.
    • Prepare and submit applications and communications with regulatory agencies as appropriate.
    • Represent study team at study initiation meetings.
    • Assist with organizing case report forms and regulatory binders.
    • Screen potential research subjects for participation in clinical trials; evaluate ongoing eligibility of research subjects’ participation in clinical trials.
    • Demonstrate an understanding of the informed consent process.
    • Obtain informed consent from research subjects as per protocol and document obtaining of informed consent in the medical record.
    • In conjunction with PI, monitor protocol enrollment goals and collaborate in the development of recruitment strategies to ensure accrual and retention within goal time frames; demonstrate knowledge of protocol endpoint definitions.
    • Assist with ensuring collection of pertinent data from internal and external sources. Monitor compliance with requirements of assigned clinical trials.
    • Obtain and ensure proper distribution of required pharmacokinetic & tissue samples.
    • Schedule, perform, and/or monitor procedures and tests per protocol requirements.
    • Ensure and coordinate correct documentation of clinical study in medical record and appropriate protocol documents. Schedule visits, tests and procedures for patients entered in clinical trials per the protocol.
    • As appropriate, ensure all required signatures are obtained on informed consent documents and validity of available informed consent documents.
    • Perform subject interviews and assessments at study visits for data collection required by protocol, as appropriate.
    • Apply pharmacologic knowledge to assist PI in determining adverse event causality and relationship to study drug/procedure. As appropriate, performs phlebotomy per policy and procedures; and documents per institutional standards.
    • Make return (~monthly) participant visits and coordination as well as, blood draws in addition to clinical assessments.
    • High degree of understanding of research and applies general analytical skills to administer the logistical implementation of assigned projects, and to identify situations requiring special attention. Utilizing this knowledge, will ensure adherence to research protocols, operating procedures, and all associated internal/external regulations.
    • Using working knowledge will assist in developing recruitment tools for assigned study(s), which include protocol/study specific data collection forms, drafting and placing approved advertisements, and contacting physicians for possible referrals.
    • Develop moderately complex tracking database/spreadsheet based on study requirements utilizing Excel, REDCap, or similar software applications.
    • Abstract data from patient medical records that requires some interpretation. Monitors data quality and accuracy as required by research protocol. Will run pre-established queries and may develop ad-hoc queries/reports as requested.
    • Utilizing working knowledge of study(s) will participate in meetings to provide operational updates, report on any operational issues, and may make recommendations for resolutions to new/outstanding operational issues. Will coordinate study(s) meetings, including developing an agenda and coordinating information and participation of individuals from other institutions.
    • Oversee budget expenditures based on the study(s) operational expectation.
    • Will act as the primary contact for study participants, including scheduling, confirming appointments, and escorting/directing to various locations on/off campus.
    • Ensure that case files and accompanying paperwork are organized and current.
    • Assists with data analysis, interpretation, manuscript and abstract preparation. Although training in statistical analysis is not a requirement, familiarity with data analysis software is a plus.
    • Opportunity for participation in scholarly activity and paper authorship.
    • Perform other duties as required.
    Qualifications:
    • Bachelor’s degree in a related field is required. Master’s degree in a related field is helpful but not required.
    • Prior research experience (both clinical and laboratory biomedical research) is highly valuable. Additional education may substitute for experience. Additional experience may substitute for education.
    • Must maintain current required research certifications during the duration of employment.
    • Completion of the JHH required training prior to the start date.
    • Ability to demonstrate knowledge and skills necessary to perform her role as it pertains to women's reproductive health research.
    • Able to prioritize workload and manage multiple projects effectively.
    • Must achieve and maintain a working knowledge of computer software specific to the department, including Microsoft Word and Excel, e-mail and internet functions and is knowledgeable of the Johns Hopkins Institutional Review Board and departmental Standard Operating Procedures.
    To apply:
    Please, submit resume and a cover letter.
    Job Type: Full-time
    Work Location:
    • One location
    Benefits:
    • Health insurance
    • Dental insurance
    • Vision insurance
    • Retirement plan
    • Paid time off
    • Parental leave
    • Professional development assistance
    • Tuition reimbursement
    This Job Is Ideal for Someone Who Is:
    • Dependable -- more reliable than spontaneous
    • Detail-oriented -- would rather focus on the details of work than the bigger picture
    • Achievement-oriented -- enjoys taking on challenges, even if they might fail
    Schedule:
    • Monday to Friday
    • No weekends

    University of Washington Cardiology RESEARCH STUDY ASSISTANT

    As a UW employee, you have a unique opportunity to change lives on our campuses, in our state and around the world. UW employees offer thei...