H-1B Visa Associate Principal Scientist Jobs
Associate Principal Scientist jobs sit squarely within H-1B visa specialty occupation territory, requiring at least a bachelor's degree in a directly related scientific discipline. Employers in pharma, biotech, and chemicals file LCAs and I-129 petitions to sponsor this role. H-1B status is granted for up to three years, extendable to a six-year maximum.
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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 inline 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 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 HTA 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.
MINIMUM QUALIFICATIONS:
- 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 QUALIFICATIONS:
- 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:
- Economic Modeling
- Epidemiology
- Health Economic Modeling
- Health Economics
- Health Technology Assessment (HTA)
- Observational Studies
- Outcomes Research
- Public Health
- Stakeholder Relationship Management
- Strategic Planning
PREFERRED SKILLS:
- Health Services Research
- Immunizations
- Infectious Disease
- Pharmacoeconomics
- Scientific Publishing
The primary location for this posting is:
USA - New Jersey - Rahway
The salary range for the primary location of this role is:
$156,900.00 - $247,000.00
This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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.
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 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
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
Employee Status:
Regular
Relocation:
Domestic
VISA Sponsorship:
Yes
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Job Posting End Date:
11/30/2026*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.
Requisition ID: R425488
See all 60+ H-1B Visa Associate Principal Scientist Jobs
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Get Access To All JobsTips for Finding H-1B Visa Sponsorship as an Associate Principal Scientist
Align your degree to the role
USCIS evaluates whether your degree field directly relates to the duties listed in the job posting. For Associate Principal Scientist roles, a degree in chemistry, biology, pharmacology, or a closely related discipline strengthens the specialty occupation argument considerably.
Verify prevailing wage before negotiating
Your employer's LCA must certify a wage at or above the prevailing wage for your SOC code and work location. Use the OFLC Wage Search to look up the wage level for your specific city before entering salary discussions.
Target companies with active H-1B LCA histories
Pharma, biotech, and contract research organizations file LCAs for scientist roles regularly. Use Migrate Mate to search employers with verified H-1B sponsorship history filtered by scientific occupations, so you're targeting companies already set up to file.
Confirm each worksite has its own certified LCA
If your role involves work at a client site, field location, or secondary lab, your employer must file a separate certified LCA for each worksite address. Raise this with HR before accepting an offer to avoid compliance gaps after you start.
Review your O*NET profile before the petition
The O*NET occupation profile for your SOC code describes typical duties and minimum education for the role. Your employer's I-129 petition should map your job duties directly to this profile to support the specialty occupation determination.
Prepare for an RFE on degree equivalency
If your degree is from outside the U.S. or is in a loosely related field, USCIS may issue a Request for Evidence. Get a credential evaluation from a NACES-member organization and document any graduate coursework or publications that reinforce your scientific qualifications before the petition is filed.
H-1B Visa Associate Principal Scientist: Frequently Asked Questions
Does an Associate Principal Scientist role qualify as an H-1B specialty occupation?
Yes, Associate Principal Scientist roles typically qualify as H-1B specialty occupations. The position requires at least a bachelor's degree in a specific scientific field such as chemistry, biology, pharmacology, or biochemistry, and the work involves applying that theoretical knowledge directly. USCIS looks at the job duties, the employer's requirements, and the industry norm to confirm the degree requirement is genuine.
Which industries sponsor H-1B visas most often for scientist roles?
Pharmaceutical manufacturers, biotechnology firms, medical device companies, contract research organizations, and specialty chemical companies file LCAs for Associate Principal Scientist positions regularly. These employers have established immigration programs and are accustomed to the LCA and I-129 process. You can browse verified sponsoring employers on Migrate Mate by occupation and location.
How long does H-1B status last for an Associate Principal Scientist?
USCIS grants H-1B status for up to three years on the initial petition. Your employer can file an extension to reach a six-year maximum. Beyond six years, further extensions are possible if you have an approved I-140 immigrant petition or a PERM labor certification that has been pending for at least 365 days, allowing you to remain in H-1B status while your green card case progresses.
What happens to my H-1B if I transfer to a different lab location?
Each worksite where you perform H-1B work requires its own certified LCA listing that specific address and the prevailing wage for that location. If your employer moves you to a new lab, a client site, or any location not covered by your existing LCA, they must file a new LCA with DOL and may need to amend your I-129 petition with USCIS before you begin work there.
Can I switch employers while on H-1B as an Associate Principal Scientist?
Yes. Under H-1B portability rules, you can start working for a new employer as soon as they file an H-1B transfer petition with USCIS, without waiting for approval, provided your current H-1B status is valid and you haven't had a gap in authorized employment. The new employer must file a fresh LCA for the new worksite and submit an I-129 petition before your first day.