Associate Director, Healthcare Quality Improvement (AD, HQI)
USA - Pennsylvania - North Wales (Upper Gwynedd), United States
Job Description
Role Summary
The Associate Director, Healthcare Quality Improvement (AD, HQI) is a core member of the Healthcare Quality Improvement team within Global Medical Proficiency and External Affairs (GMPEA), that serves as an internal expert on implementation science methodologies and partners cross-functionally to support the development of implementation science strategies contributing to the adoption of evidence-based interventions.
The AD HQI reports directly to the Healthcare Quality Improvement Center of Excellence Team Lead and provides expert guidance on the design and execution of implementation science research, and advises on the dissemination of findings to advance evidence-based healthcare policy and practice.
Responsibilities and Primary Activities
Provides support on the integration of implementation science principles into global medical and scientific, and outcomes research initiatives and ensures alignment at the regional and local level.
Provides expertise and advises cross-functional teams on the development and evaluation of implementation research proposals and initiatives, supporting the development of strategies included as part of Value & Implementation (V&I) planning.
Enables operationalization of implementation science opportunities providing input to ensure alignment; establishing pathways and mechanisms in partnership with legal, compliance and operations functions, to enable execution of implementation science initiatives.
Supports development and execution of companywide strategy on global training and roll out plans related to implementation science.
Facilitates consistent and appropriate oversight of implementation science activities serving as a subject matter expert reviewer as part of internal review committees (e.g., quality improvement/performance improvement activities, grants, Company investigator studies and publications).
Serves as an expert advisor to internal teams by providing comprehensive consultations on the design and execution of implementation science research protocols (e.g., study design methodologies, feasibility assessments).
Advises on the dissemination of implementation science findings and shares research dissemination best practices to support evidence-based healthcare policy and practice.
Supports external engagements with professional medical societies and organizations on topics related to implementation science.
Identifies, manages, and collaborates with external agencies to support implementation science activities for Our Company.
Attends and supports scientific and medical meetings and prepares post-meeting deliverables.
Required Qualifications, Skills, & Experience
Minimum
BA/BS degree.
5 years of experience in implementation research (e.g., writing and developing research proposals and protocols).
Working knowledge and expertise in implementation science concepts and methodologies (e.g., implementation frameworks, outcomes, and strategies).
Strong understanding of healthcare systems and policy, as well as experience working in a global or multi-country context.
Project and vendor management proficiency, strong communication skills, persuasive skills, and the ability to lead without direct authority over a continuum of stakeholders.
Thorough understanding of ethical guidelines relevant to the pharmaceutical industry.
Ability to work in a complex organization environment and to effectively operate in a team-oriented global structure.
Preferred
MPH, PhD, or credentialed healthcare professional degree (PharmD, NP, PA).
Relevant experience leading implementation science initiatives within pharmaceutical industry.
Proven track record of publishing in peer-reviewed journals and presenting at scientific conferences on implementation science topics.
Flexible and entrepreneurial attitude to support a newer team and establish new processes.
Experience in creating and implementing training programs.
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U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.
Expected US salary range:
$169,700.00 - $267,200.00Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
25%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
04/26/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
ApplyJob Profile
Colorado Hybrid Hybrid work Hybrid work model On-site Puerto Rico residents only US and Puerto Rico residents only
Benefits/PerksBonus eligibility Equal opportunity Flexible work Flexible work arrangements Healthcare Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Meetings Paid holidays Retirement benefits Sick Days Training programs Vacation
Tasks- Advise on research proposals
- Communication
- Compliance
- Consult on research protocols
- Engage with external agencies
- Execution
- Facilitate training and roll out plans
- Feasibility
- Innovation
- Planning
- Support implementation science integration
Best Practices Communication Compliance Cross-functional Teams Design Development Education Ethical guidelines Evaluation Execution Healthcare Healthcare policy Healthcare quality Healthcare systems Implementation Science Inclusion Innovation Integration Management Manufacturing Medical Methodologies Operations Organization Outcomes Research Performance Improvement Persuasion Persuasive Pharmaceutical Pharmaceutical Industry PharmD PhD Planning Policy Project Management Protocols Publications Quality Quality improvement Research Research Initiatives Research proposals Science Strategy Study Design Teams Training Training Programs Vendor Management Writing
Experience5 years
EducationAS Associate B.A. BA/BS BA/BS degree B.S. Business Degree Development Health Care Management MPH N.P. PA Pharm.D Ph.D. Professional Degree Relevant experience Science
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9