Associate Principal Scientist, Outcomes Research, HIV

Merck; North Wales (Montgomery County); Hybrid; USD 157,000 - 247,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) retirement plan

Paid holidays

Job summary

Merck invites applications for an Associate Principal Scientist/Associate Director, Value & Implementation (V&I) Outcomes Research, HIV. This role plans and manages real-world and economic evidence studies to support reimbursement and HTA submissions globally.

You will design studies, author protocols, and develop data collection instruments for robust analyses. Responsibilities include AMCP and Global Value dossiers, vendor management, and collaboration with clinical development, medical

Qualifications

• Master’s degree in health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, or pharmacy administration.
• 1-3 years experience post-master’s degree or 1+ year post-doctoral degree.

Responsibilities

• Plan and manage real-world and economic evidence activities for in-line and pipeline products.
• Design studies; author protocols; develop questionnaires, CRFs, data analysis plans, and final reports.
• Develop AMCP dossiers for U.S. payers and Global Value Dossiers.
• Coordinate with cross-functional teams to communicate outcomes data to stakeholders.
• Manage contracts, budgets, and vendor relationships in line with policies and regulations.

Skills

Epidemiology

Health Economics

Meta-Analysis

Observational Studies

Outcomes Research

Pharmacoeconomics

Project Management

Prospective Studies

Research Protocols

Scientific Presentations

Scientific Writing

Stakeholder Relationship Management

Education

Master’s degree in health services research / outcomes research / epidemiology / public health / health economics

Doctoral degree (PhD, MD, DrPH, ScD, PharmD) in a relevant discipline

Job description

Job Description

Associate Principal Scientist/Associate Director, V&I Outcomes Research, HIV

Role Summary

• The Associate Principal Scientist/Associate 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.
• Under the guidance of a senior leader, this position has primary responsibility for planning/managing real-world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment/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 dossiers for U.S. payers, and Global Value Dossiers for use by local subsidiaries in their health technology assessment submissions. The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates. The incumbent may supervise external vendors or partners to execute these activities. The incumbent may have direct interactions with health technology assessment agencies, reimbursement decision makers, or national immunization technical advisory groups.

Responsibilities and Primary Activities

• 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 strategy 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 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 customers.
• 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

• Master’s degree in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration).
• One to three years experience post master’s degree or one or more years experience post doctoral 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).

Required Skills:

Epidemiology, Health Economics, Meta-Analysis, Observational Studies, Outcomes Research, Pharmacoeconomics, Project Management, Prospective Studies, Research Protocols, Scientific Presentations, Scientific Writing, Stakeholder Relationship Management

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)

The salary range for this role is

$156,900.00 – $247,000.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s 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 https://jobs.merck.com/us/en/compensation-and-benefits.

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

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

10/17/2026