Principal Scientist/Director, V&I Outcomes Research (Pneumococcal Vaccines)
Principal Scientist/Director, V&I Outcomes Research (Pneumococcal Vaccines)
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$ 187000 - 294400
1 Vacancy
Job Description
Job Description
Role Summary
The Principal Scientist/Director Value & Implementation (V&I) Outcomes Research position resides in the V&I organization which includes Global Medical and Scientific Affairs as well as Outcomes Research and will support Pneumococcal Vaccines.
Under the guidance of a senior leader this position supports value evidence outcomes research plans and real-worldevidence activities for in-line and pipeline products to meet the value evidence needs of clinicians payers policymakers health technology assessment (HTA)/reimbursement agencies and health systems globally.
Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology treatment patterns health-care resource utilization and costs physician and patient satisfaction surveys clinical and patient- reported outcomes assessments systematic reviews and meta-analyses and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for U.S. payers and Global Value Dossiers for use by local subsidiaries in their HTA submissions.
The incumbent is expected to contribute to product development and marketing strategies throughout the lifecycle to ensure that product value is defined and developed to achieve optimal market/patient access and reimbursement. The incumbent is expected to work cross-functionally with clinical development medical affairs biostatistics market access commercial and country affiliates and may have direct interactions with HTA agencies reimbursement decision makers and national immunization technical advisory groups.
Responsibilities and Primary Activities
Partners with Medical Affairs counterparts to develop execute and deliver on the Value and Implementation (V&I) plan for pneumococcal vaccines.
Helps achieve / sustain reimbursement and market access for the program and indications under their responsibility.
Critically assesses drivers and barriers to reimbursement and market access and provides input into clinical regulatory payer/access marketing and evidence generation strategies and programs.
In collaboration with internal teams and external partners designs studies; authors study protocols; and develops measurement questionnaires case report forms data analysis plans final study reports scientific presentations and publications.
Responsible for study-related contracting budgets and vendor/partner management and ensures study conduct is aligned with company Policies and standard operating procedures (SOPs) and world-wide regulations and standards including Good Pharmacoepidemiology Practice (GPP) for applicable work.
Develops American Managed Care Pharmacy (AMCP) dossiers for U.S. payers and Global Value Dossiers.
Develops supplementary clinical data package in close partnership with markets and HTA statistics group for submission to HTA agencies.
Supports country affiliates to understand local evidence generation needs adapts health economic evaluations and customizes outcomes research documents such as protocols and reimbursement dossiers according to local requirements.
Works closely with cross-functional teams to effectively communicate outcomes research and health economic modelling data internally and to external stakeholders.
Maintains awareness of new scientific and methodological developments within therapeutic area.
Builds relationships with scientific experts worldwide.
Presents outcomes research data at national and international congresses and publishes articles in scientific journals.
Required Qualifications Skills and Experience
Minimum
Masters degree in relevant discipline (health services research outcomes research epidemiology public health health economics pharmacoeconomics pharmacy administration).
Four or more years of experience post degree.
Preferred
Doctoral degree (PhD MD DrPH ScD PharmD) in relevant discipline (health services research outcomes research epidemiology public health health economics pharmacoeconomics pharmacy administration).
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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 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 salary range for this role is
$187000.00 - $294400.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive if applicable.
We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
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:
DomesticVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aRequired Skills:
Biostatistics Clinical Development Communication Data Management Epidemiology Health Economics Health Outcomes Research Health Technology Assessment (HTA) Management Process Marketing Strategies Medical Affairs Neuroanatomy Outcomes Research Pathophysiology Pharmacokinetics Researching Social Collaboration Stakeholder Relationship Management Strategic PlanningPreferred Skills:
Job Posting End Date:
08/2/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Director
Employment Type
Full-Time
