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    Medication Safety Specialist - Membership

    Ismp
    5+ years
    Not Disclosed
    Remote, USA
    10 Aug. 14, 2024
    Job Description
    Job Type: Full Time Education: MS degree in health sciences, MSN, DNP, PharmD, or equivalent Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Position: Medication Safety Specialist (Per Diem)

    Location: Corporate Headquarters - Plymouth Meeting, PA (Fully Remote)

    Education Level: Doctorate/Professional Degree Required

    Travel Percentage: 10%

    Job Shift: Day

    Job Category: Pharmaceutical

    About ISMP

    The Institute for Safe Medication Practices (ISMP) is a 501(c)(3) nonprofit organization dedicated to preventing medication errors. For over 25 years, ISMP has been a leader in improving patient safety and supporting healthcare professionals through its advocacy, education, and safety initiatives. ISMP’s efforts have led to significant changes in clinical practices, public policy, and drug labeling.

    In 2020, ISMP affiliated with ECRI, forming the ECRI and ISMP Patient Safety Organization (PSO). This affiliation combines the expertise of both organizations to enhance healthcare safety and support providers, patient advocates, and governments.

    ISMP operates independently of advertising revenue and relies on charitable donations, educational grants, and volunteer contributions.

    Position Summary

    The Medication Safety Specialist serves as a subject matter expert (SME) in medication use processes and safe medication practices. This role involves contributing to membership and consulting activities, educational programs, data analysis, and advocacy efforts. The Specialist will author and edit content for ISMP publications, research proposals, safety projects, and tools, and will analyze error reports from ISMP and ECRI's reporting programs. This per diem position does not guarantee a set number of hours and will vary based on business needs.

    Essential Functions

    Subject Matter Expert (SME) in Safe Medication Practices:

    • Provide expertise on medication use processes and safety practices.
    • Engage in membership and consulting activities, educational programs, and special projects.
    • Author and edit content for ISMP publications, including guidelines, self-assessments, and best practice statements.
    • Offer guidance to healthcare practitioners, consumers, ISMP Fellows, and students.

    Error Reporting Programs and ECRI & ISMP PSO:

    • Review and analyze confidential reports of hazardous conditions and medication errors from various ISMP programs and the ECRI & ISMP PSO.
    • Identify the causes of medication errors and collaborate on ISMP’s responses and recommendations.
    • Develop and implement action agendas to prevent or mitigate medication errors.

    Collaboratives, Summits, Consultations, and Other Projects:

    • Participate in collaboratives, summits, and consultations.
    • Conduct risk assessments and contribute to the development and review of safety tools and resources.
    • Coordinate and edit content for new or revised safety guidelines and best practice statements.

    Education:

    • Create and deliver presentations on medication safety topics for various pharmacy practices.
    • Mentor new employees, ISMP Fellows, students, residents, and international guests.

    Additional Responsibilities:

    • Perform other duties as assigned.

    Qualifications

    Experience:

    • Minimum of 5 years of clinical experience.
    • Expertise in medication safety, error-prevention principles, and risk management methodologies (e.g., root cause analysis, failure modes and effects analysis).
    • At least 3 years of experience in implementing safety practices, managing projects, and utilizing healthcare risk management tools.
    • Experience in writing newsletters, proposals, and peer-reviewed articles.
    • Preferred experience in government or foundation-funded research projects and report writing.

    Education:

    • MS degree in health sciences, MSN, DNP, PharmD, or equivalent.

    Computer Skills:

    • Proficient in Microsoft Office 365 Suite.

    Certifications & Licenses:

    • Current professional licensure.
    • Specialty certification in patient safety, medication safety, or quality/risk preferred.

    Physical Demands

    This role is remote and requires the individual to remain in a stationary position for most of the workday. The position involves operating standard office equipment and communicating information effectively in written and oral forms.

    ADA Statement

    ECRI is committed to equal employment opportunities (EEO) for all employees and applicants without regard to race, color, religion, sex, national origin, age, disability, genetics, sexual orientation, gender identity, or veteran status. We value diversity and believe it enhances our success. ECRI adheres to all applicable federal, state, and local laws governing nondiscrimination in employment.

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