Associate Director, Outcomes Research - Lung Cancer
msdNorth Wales, PA
$156,900 per year
APPLYAssociate Director, Outcomes Research - Lung Cancer
msdNorth Wales, PALead L6
$156,900 per year
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)Administration of Public Health ProgramsResearch and Development in Biotechnology (except Nanobiotechnology)
APPLY NOWUnder the guidance of a senior leader, the Associate Director, Outcomes Research position in lung cancer has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products in lung cancer to meet the value evidence needs of clinicians, payers, policymakers, 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, healthcare 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 US payers, and Global Value Dossiers for use by local subsidiaries in their HTA 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 (HTA) agencies, and reimbursement decision makers.
Primary Responsibilities:
Participate in value evidence teams and serves as outcomes research representative on cross-functional regional and global teams.
Critically assess drivers and barriers to reimbursement and market access, and provide input into clinical, regulatory, payer/access, marketing and evidence generation strategy and programs.
In collaboration with internal teams and external partners, design studies, author study protocols, develop 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.
Develop American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers.
Develop supplementary clinical data package in close partnership with markets and HTA statistics group for submission to HTA agencies.
Support country affiliates to understand local evidence generation needs, adapt health economic evaluations, customize outcomes research documents, such as protocols and reimbursement dossiers, according to local requirements.
Work closely with cross functional teams to effectively communicate outcomes research and health economic modelling data internally and to external customers.
Maintain awareness of new scientific and methodological developments within therapeutic area.
Build relationships with scientific experts worldwide.
Present outcomes research data at national and international congresses and publish articles in scientific journals.
Required Education:
Masters degree (MSc, MPH) in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration).
Preferred EducationDoctoral degree (PhD, DrPH, ScD, PharmD) in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration).
Required Experience:
A minimum of 1 year of relevant work experience with a doctoral degree.
A minimum of 3 years of relevant work experience with a master's degree.
Required SkillsEpidemiology
Evidence Gathering
Health Economics
Health Services Research
Meta-Analysis
Observational Studies
Outcomes Research
Patient Reported Outcomes
Pharmacoeconomics
Prospective Studies
Real World Data
Real World Evidence (RWE)
Retrospective Analysis
Scientific Presentations
Scientific Writing
Stakeholder Relationship Management
Strategic Planning
Study Design
Equal Employment OpportunityOur company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.
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 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
Salary and Benefits:
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. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days
Location & Working ConditionsSan 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: Yes
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.
About the Company:
Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
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Level
Lead L6
Salary
$156,900 per year
Location
North Wales, PA
Occupation
Medical Scientists, Except Epidemiologists
Industry
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
Posted
2 days ago