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U.S. Department of Veterans Affairs

Pharmacist (Facility Program Manager) - Medication Safety, Quality and Research

sioux falls, SD

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About this opportunity

U.S. Department of Veterans Affairs lists this Pharmacist (Facility Program Manager) - Medication Safety, Quality and Research opportunity in sioux falls, South Dakota. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Summary

The Pharmacy Medication Safety - Quality and Research Program Manager must be a licensed pharmacist - preferably with a Pharm.D. or equivalent experience. The incumbent will function at the highest level of clinical practice working independently based on their scope of practice - if applicable. The incumbent will develop - organize - coordinate and manage the Medication Safety - Quality and Research programs at all points of care within the Sioux Falls VA Health Care System (SFVA HCS).

The Pharmacy Medication Safety - Quality and Research Program Manager must be a licensed pharmacist - preferably with a Pharm.D. or equivalent experience. The incumbent will function at the highest level of clinical practice working independently based on their scope of practice - if applicable. The incumbent will develop - organize - coordinate and manage the Medication Safety - Quality and Research programs at all points of care within the Sioux Falls VA Health Care System (SFVA HCS).

Qualifications

United States Citizenship: Non-citizens may only be appointed when it is not possible to recruit qualified citizens in accordance with VA Policy

Education: Graduate of an Accreditation Council for Pharmacy Education (ACPE) accredited College or School of Pharmacy with a baccalaureate degree in pharmacy (BS Pharmacy) and/or a Doctor of Pharmacy (Pharm.D.) degree

NOTE: Prior to 2005 ACPE accredited both baccalaureate and Doctor of Pharmacy terminal degree program

Today the sole degree is Doctor of Pharmacy

Licensure: Full - current and unrestricted license to practice pharmacy in a State - Territory - Commonwealth of the United States (i.e - Puerto Rico) - or the District of Columbia

Exception: Non-licensed pharmacists who otherwise meet the eligibility requirements may be given a temporary appointment at the entry level as a Graduate Pharmacist under the authority of 38 U.S.C.

7405(c)(2)(B)

The appointing official may waive the requirement of licensure for a period not to exceed 2 years for a pharmacist that provides care under the supervision of a licensed pharmacist

Foreign Education: Graduates of foreign pharmacy degree programs meet the educational requirement if the graduate is able to provide proof of achieving the Foreign Pharmacy Graduate Examination Commission (FPGEC) Certification - which includes passing the Foreign Pharmacy Graduate Equivalency Examination (FPGEE) and the Test of English as a Foreign Language Internet-Based Test (TOEFL iBT)

English Language Proficiency: Pharmacists must be proficient in spoken and written English as required by 38 U.S.C. 7402(d) - and 7407(d)

May qualify based on being covered by the Grandfathering Provision as described in the VA Qualification Standard for this occupation (only applicable to current VHA employees who are in this occupation and meet the criteria)

Grade Determinations: GS-13 Pharmacist (Facility Program Manager) Experience

In addition to the GS-12 requirements - must have 1 year of experience equivalent to the next lower grade level

AND Pharmacists assigned to this position must demonstrate the following KSAs: a

Ability to communicate orally and in writing to persuade and influence clinical and management decisions

b

Expert understanding of regulatory and quality standards for their program area

c

Ability to solve problems - coordinate and organize responsibilities to maximize outcomes in their program area or area of clinical expertise

d

Expert knowledge of a specialized area of clinical pharmacy practice or specialty area of pharmacy

e

Advanced skill in monitoring and assessing the outcome of drug therapies - including physical assessment and interpretation of laboratory and other diagnostic parameters

Reference: For more information on this qualification standard - please visit

The full performance level of this vacancy is GS-13

The actual grade at which an applicant may be selected for this vacancy is GS-13

Physical Requirements: You will be asked to participate in a pre-employment examination or evaluation as part of the pre-employment process for this position

Questions about physical demands or environmental factors may be addressed at the time of evaluation or examination.

Duties

NOTE: The 2-page Resume requirement does not apply to this position

The position requires extensive knowledge and skill in utilizing Medication Safety databases and informatics tools for patient safety/informatics analysis

The incumbent will provide a consistent point of contact for multidisciplinary and interdepartmental process improvement efforts in the areas of medication safety and quality - and will serve as a facility champion

This role will directly contribute to the health care system's commitment as a high reliability organization

The pharmacist may also function in the pharmacy to meet patient care needs

Functions of Position: A

Program Management - Medication Safety Manages data collection - analysis - and review of medication safety events and practices including reporting of adverse events in JPSR - VA ADERS - and VistA ADR tracking system

Reviews and assesses compliance with VHA Directives/Handbooks - USP - FDA - DEA - AWE - OIG and Joint Commission standards

Assists with the development and implementation of policies and procedures to ensure compliance with regulatory and accreditation medication safety standards

Utilizes resources published by the National Center for Patient Safety (NCPS) - Pharmacy Benefits Management (PBM) - the Center for Medication Safety (VA MedSAFE) - the Institute for Safe Medication Practices (ISMP) - and the FDA - disseminates information on medication related patient safety issues to appropriate clinical staff and committees and collects and analyzes SFVA HCS data as necessary

B

Program Management - Quality Management Maintaining a system of internal reviews that ensure that service programs operate at a satisfactory level of performance and compliance with VHA Directive/Handbooks - regulatory bodies - and accreditation organizations

Collaboration with pharmacy management and clinical ICCs to coordinate pharmacy service continuous readiness for all regulatory bodies including The Joint Commission - LTCI - CARF - AWE - OIG - VACO - and VISN 23

Ensures that all pharmacy programs (to include Compounded Sterile Preparations - Anticoagulation - Pharmacoeconomics - Drugs Supply Chain - Controlled Substance - Clinical Pharmacy Programs) are in full compliance and readiness in regard to all applicable VHA regulations - policies - directives - and handbooks

C

Administrative Program Services Assists with the management of the Medication Recall and Drug Safety Alert System

Develops and updates policies and procedures defining operational requirements of Medication Safety and Quality Program

Assists with developing and updating all policies and procedures within the pharmacy enterprise

D

Pharmacist Duties Provide routine patient care in clinical settings as directed

Participates in staff pharmacy duties - including order verification - medication preparation - dispensing in inpatient and outpatient settings

Interacts with treatment team members to optimize drug treatment

develops and assesses target outcomes

Communicates effectively in meetings - in personal conversations - and in written progress notes or consultations

E

Pharmacy Investigational Drug Service Serves as an authoritative information source on investigational drugs and their utilization in therapy

This includes the interpretation and dissemination of information about investigational drugs to pharmacists - nurses - and medical staff via bulletins - newsletters - and policy memos as necessary or required

Serves as a consultant on regulatory matters to all investigators

Ensures compliance with appropriate regulatory bodies (i

Institutional Review Board - Research and Development - AAHRPP - VHA Directives and Handbooks)

Coordinates patient care and addresses procedural concerns when patients are admitted to the Medical Center and are currently enrolled - or previously have been previously enrolled in investigational studies

F

Education: Collaborates with Pharmacy Management and Patient Safety on pharmacy-related training and development - to promote the learning experience and improve the performance of providers - pharmacists - pharmacy technicians - pharmacy residents - medical residents and students

Develops and implements of formal and informal drug education/clinical consultation to medical - surgical - nursing - and pharmacy staff in the form of in-services and continuing education programs

Interfaces with health-care providers and administrators to ensure compliance with established pharmacy policies and procedures

G

Research May be involved in designing and conducting research studies or assist in the same

Proposals for research must be submitted to the IRB and Research and Development Committee

Work Schedule: Monday - Friday

7:30am - 4:00pm Telework: Not available Virtual: This is not a virtual position

Functional Statement #: Relocation/Recruitment Incentives: Not authorized Permanent Change of Station (PCS): Not authorized

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Worksite address

sioux falls, SD, 57102, US

Who can apply

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