Associate Principal Scientist/Associate Director, Outcomes Research Division / Area: Value and Implementation Workday Job Profile: Consult with Global Human Resources Band / Pathway / Level: Consult ...
Associate Principal Scientist/Associate Director, Outcomes Research Division / Area: Value and Implementation Workday Job Profile: Consult with Global Human Resources Band / Pathway / Level: Consult ...
This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to ...
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Rahway, NJ · On-site
$156K - $247K/yr
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Associate Principal Scientist (Associate Director) - Outcomes Research - Hematology
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$156K - $247K/yr
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Associate Principal Scientist (Associate Director) - Outcomes Research - Hematology
North Wales, PA · On-site
$156K - $247K/yr
This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to ...
Associate Principal Scientist (Associate Director) - Outcomes Research - Hematology
Rahway, NJ · On-site
$156K - $247K/yr
This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to ...
Associate Principal Scientist (Associate Director) - Outcomes Research - Hematology
Rahway, NJ · On-site
$156K - $247K/yr
This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to ...
This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to ...
This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to ...
The Associate Director of Epidemiology and Outcomes Research (ADEOR) will be involved in managing the day to day activities of the Clinical Research Managers across the registries. Critical skills ...
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Associate Director, Health Economics & Outcomes Research
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About the Role Secura Bio is seeking a talented and motivated Associate Director of Health Economics and Outcomes Research to join our Medical Affairs organization. The ideal candidate will ...
Associate Director, Health Economics & Outcomes Research
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Waltham, MA · On-site
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Cranbury, NJ · On-site
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Health Economics & Outcomes Research Associate Director, Pain
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Health Economics & Outcomes Research Associate Director, Pain
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The Health Economics & Outcomes Research Associate Director will participate in leading the development and execution of Health economics and outcomes research studies in support of Vertex's products.
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Philadelphia, PA · On-site +1
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Director Outcomes Research information
See salary details
$57.5K - $73.2K
1% of jobs
$73.2K - $89K
4% of jobs
$89K - $104.7K
5% of jobs
$104.7K - $120.4K
9% of jobs
$132.2K is the 25th percentile. Wages below this are outliers.
$120.4K - $136.1K
8% of jobs
$136.1K - $151.9K
5% of jobs
$151.9K - $167.6K
2% of jobs
$167.6K - $183.3K
1% of jobs
$183.3K - $199K
1% of jobs
$199K - $214.8K
0% of jobs
The median wage is $218.1K / yr.
$214.8K - $230.5K
63% of jobs
$57.5K
$191.3K
$230.5K
How much do director outcomes research jobs pay per year?
What are some typical projects or responsibilities for a Director Outcomes Research?
Directors of Outcomes Research often lead multi-disciplinary teams in designing and executing studies that measure healthcare interventions' real-world effectiveness, safety, and economic value. Responsibilities typically include overseeing study protocols, managing data collection and analysis, developing publications or presentations, and collaborating closely with internal groups such as medical affairs, clinical development, and market access. The director also engages with external stakeholders, including regulatory bodies and academic partners, to ensure research aligns with industry standards and organizational strategy. This role demands both strategic oversight and hands-on involvement in research projects, offering a dynamic and intellectually stimulating work environment.
What does a Director of Outcomes Research do?
A Director of Outcomes Research leads the design, execution, and analysis of studies that assess the real-world effectiveness, value, and impact of healthcare interventions. They collaborate with cross-functional teams, including clinical, medical affairs, and health economics experts, to generate evidence that supports regulatory approval, market access, and reimbursement decisions. Their work involves leveraging data from clinical trials, real-world evidence, and epidemiological studies to inform healthcare policies and improve patient outcomes. Additionally, they ensure that research aligns with industry standards, regulatory requirements, and payer expectations.
What are the key skills and qualifications needed to thrive in the Director Outcomes Research position, and why are they important?
To thrive as a Director Outcomes Research, you typically need an advanced degree in a health-related or quantitative field, experience in outcomes research or health economics, and a strong understanding of epidemiological study design and data analysis. Familiarity with statistical analysis software (such as SAS, R, or STATA), real-world evidence platforms, and relevant certifications like CPH (Certified in Public Health) are highly valuable. Exceptional leadership, communication, and stakeholder management skills help drive cross-functional research initiatives and facilitate collaboration. These competencies are crucial for generating evidence that informs healthcare decision-making, supports organizational goals, and advances patient outcomes.

Associate Principal Scientist (Associate Director) -Outcomes Research
Rahway, NJ • On-site
Full-time
Medical, Dental, Vision, Retirement, PTO
This job post has expired 1 day ago. Applications are no longer accepted.
Merck rating
7.8
Based on 50 frontline employees who took The Breakroom Quiz
44th of 74 rated pharmaceutical
Job description
Title:
Associate Principal Scientist/Associate Director, Outcomes Research
Division / Area:
Value and Implementation
Workday Job Profile:
Consult with Global Human Resources
Band / Pathway / Level:
Consult with Global Human Resources
Workday Job Family ID:
Consult with Global Human Resources
Role Summary
- Under the guidance of a senior leader, an Associate Principal Scientist/Associate Director, 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, 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, reimbursement decision makers, or national immunization technical advisory groups.
Responsibilities and Primary Activities
- Participates in value evidence teams and serves as outcomes research representative on cross-functional regional and global teams
- Critically assesses 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, designs studies, authors study protocols, 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 to ensure 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 US 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, 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, & Experience
Minimum
Masters degree (MSc, MPH) in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration)
1-3 years post degree
Preferred
Doctoral degree (PhD, DrPH, ScD, PharmD) in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration)
Required Skills:
Data Management, Researching, Stakeholder Relationship Management, Strategic Planning
Preferred Skills:
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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:
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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.
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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.
You can apply for this role through https://jobs.merck.com/us/en (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
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:
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:
07/18/2026
*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.
About Merck
Sourced by ZipRecruiter
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Rahway, NJ, US