Outcomes Research Manager – Latin America
Merck & Co.
This listing was originally posted on Merck & Co.'s careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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**Fixed-term position (1 year + 1 year), with the possibility of permanent employment
Job Responsibilities:
Under the guidance of the Director, Outcomes Research – Latin America, the Senior Scientist, Outcomes Research. This role will contribute to evidence generation across Specialty, General Pharma, and Infectious Diseases, supporting the translation of global integrated evidence strategies into regionally relevant activities through the design, execution, and dissemination of outcomes research and real‑world evidence (RWE) across Latin America.
The position focuses on delivering real‑world and health outcomes evidence to inform decision‑making by internal stakeholders and external audiences, including clinicians, payers, policymakers, and healthcare system.
Job Responsibilities
Support the design, execution, and delivery of real‑world evidence and outcomes research studies, including retrospective database studies, registries, and prospective observational studies aligned global V&I strategies
Apply epidemiology, HEOR, and pharmacoepidemiology methods to generate robust and decision‑relevant evidence
Provide input into value evidence strategies that inform access, reimbursement, and policy discussions
Contribute to evidence planning across the product lifecycle, including post‑authorization and Phase IV studies
Support end‑to‑end study execution, including protocol development, analysis plans, data interpretation, and reporting
Contribute to the adaptation and application of global evidence frameworks that reflect country‑specific healthcare systems and data environments.
Provide scientific input to V&I goals, plans, and evidence strategies,
Act as study lead for assigned outcomes research and RWE studies, with accountability for study execution, including vendor oversight, budgets, timelines, and deliverables, in compliance with company policies, SOPs, and Good Pharmacoepidemiology Practice (GPP).
Communicate study results through scientific abstracts, peer‑reviewed publications, and presentations at regional and international congresses.
Contribute to training and capability building across regional and local teams.
Provide scientific mentorship and support collaborative project execution.
Leadership Skills Needed to Be Successful in This Role
Scientific collaboration: Working effectively across functions, countries, and cultures to deliver shared evidence goals.
Analytical thinking: Interpreting quantitative and qualitative outcomes data to inform study design and evidence generation.
Communication: Translating complex scientific concepts for internal and external audiences.
Learning agility: Adapting to evolving methodologies, data sources, and evidence expectations.
Execution focus: Managing priorities, timelines, and deliverables across multiple concurrent projects
Position Qualifications:
Education Minimum Requirement:
Master’s degree in medicine, public health, pharmacy, or economics
Required Experience and Skills:
Demonstrated expertise in planning and managing real-world evidence activities, including design and implementation of clinical, epidemiological and cost studies
Proven track record of success in planning and managing real-world evidence activities, including design and implementation of primary and secondary studies (database and chart-review), epidemiological studies, and cost studies
Knowledge of principles of health economic modelling
Excellent interpersonal, communication and strategic thinking skills
Professional proficiency in English and Spanish or Portuguese.
Preferred Experience and Skills:
International experience working in multiple countries in Latin America.
Experience in the pharmaceutical industry, CROs, or consulting firms.
LaboratoriesBR
Required Skills:
Business Decisions, Clinical Study Design, Data Management, Epidemiology, Health Outcomes, Learning Agility, Outcomes Research, Protocol Development, Researching, Scientific Study Design, Stakeholder Relationship Management, Strategic Planning, Strategic ProcurementPreferred Skills:
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Search Firm Representatives Please Read Carefully
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:
Project Temps (Fixed Term)Relocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
06/4/2026*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.
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