Healthcare Jobs at AbbVie with Visa Sponsorship
Healthcare jobs at AbbVie span clinical, regulatory, medical affairs, and pharmacovigilance functions, with consistent sponsorship activity across H-1B visa, E-3 visa, TN visa, and Green Card pathways. If you're targeting a Healthcare role at AbbVie, the company has a demonstrated pattern of supporting international candidates through the full hiring and visa process.
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About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company objectives.
Responsibilities:
- Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or devices.
- Functions with a moderate degree of autonomy on draft materials but relies on review by subject matter experts and more senior writers for verification. Develop knowledge and understanding of submission strategies.
- Coordinates the review, approval, and quality control of other functions involved in the production of clinical and regulatory projects. Arranges and conducts review meetings with the team.
- Produces and maintains clinical and regulatory documents focusing on quality and compliance and ensures delivery within project timelines. Develops understanding of project management concepts and accepts greater responsibility for driving submission objectives.
- Develops knowledge of US and international regulations, requirements, and guidelines pertaining to the preparation of regulatory documentation. Understands and uses guidance associated with preparation of regulatory documentation.
- Participates in execution of tactical process improvements.
- Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
- Works closely with leadership and R&D Quality Assurance to address inquiries and draft responses, supporting an inspection-ready approach.
Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required.
Qualifications
- A minimum of 4+ years of bio-pharmaceutical industry experience in global pharma, biotech, life science, or healthcare authority delivering medicines/therapies to a broad market across various therapeutic areas.
- Bachelor's Degree or higher required; scientific discipline preferred.
- Outstanding written and oral communication skills, with a comprehensive knowledge of medical and scientific terminology across multiple therapeutic areas.
- Proficient in assimilating and analyzing complex data.
- Experience writing and editing clinical and regulatory documents following guidelines and regulations, such as ICH guidelines, GCP, and other regulatory requirements. Familiarity with industry standards like CONSORT and PRISMA guidelines. EU and US device writing experience is a plus.
- Understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory requirements, and medical terminology across functional teams and multiple contributors.
- Excellent writing skills. Effectively communicates complex scientific and medical information to various stakeholders.
- Ability to oversee multiple projects simultaneously and collaborate with cross-functional teams. Strong organizational, time management, and problem-solving skills.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company objectives.
Responsibilities:
- Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or devices.
- Functions with a moderate degree of autonomy on draft materials but relies on review by subject matter experts and more senior writers for verification. Develop knowledge and understanding of submission strategies.
- Coordinates the review, approval, and quality control of other functions involved in the production of clinical and regulatory projects. Arranges and conducts review meetings with the team.
- Produces and maintains clinical and regulatory documents focusing on quality and compliance and ensures delivery within project timelines. Develops understanding of project management concepts and accepts greater responsibility for driving submission objectives.
- Develops knowledge of US and international regulations, requirements, and guidelines pertaining to the preparation of regulatory documentation. Understands and uses guidance associated with preparation of regulatory documentation.
- Participates in execution of tactical process improvements.
- Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
- Works closely with leadership and R&D Quality Assurance to address inquiries and draft responses, supporting an inspection-ready approach.
Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required.
Qualifications
- A minimum of 4+ years of bio-pharmaceutical industry experience in global pharma, biotech, life science, or healthcare authority delivering medicines/therapies to a broad market across various therapeutic areas.
- Bachelor's Degree or higher required; scientific discipline preferred.
- Outstanding written and oral communication skills, with a comprehensive knowledge of medical and scientific terminology across multiple therapeutic areas.
- Proficient in assimilating and analyzing complex data.
- Experience writing and editing clinical and regulatory documents following guidelines and regulations, such as ICH guidelines, GCP, and other regulatory requirements. Familiarity with industry standards like CONSORT and PRISMA guidelines. EU and US device writing experience is a plus.
- Understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory requirements, and medical terminology across functional teams and multiple contributors.
- Excellent writing skills. Effectively communicates complex scientific and medical information to various stakeholders.
- Ability to oversee multiple projects simultaneously and collaborate with cross-functional teams. Strong organizational, time management, and problem-solving skills.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
See all 42+ Healthcare Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Healthcare Jobs at AbbVie.
Get Access To All JobsTips for Finding Healthcare Jobs at AbbVie
Align your credentials to AbbVie's therapeutic areas
AbbVie's Healthcare hiring concentrates in immunology, oncology, neuroscience, and aesthetics. Frame your clinical, regulatory, or medical affairs background around one of these areas before you apply. Generic pharma experience is harder to place than targeted expertise.
Distinguish specialty occupation early in applications
For H-1B sponsorship, USCIS requires the role to qualify as a specialty occupation. Healthcare roles at AbbVie in pharmacovigilance, clinical operations, or medical science liaising typically meet this bar, but your application materials should make the degree-to-role connection explicit.
Target roles where AbbVie files LCAs consistently
DOL Labor Condition Application filings are public record. Check OFLC disclosure data to see which Healthcare job titles AbbVie has sponsored most recently. This tells you where sponsorship infrastructure already exists and where hiring managers are accustomed to the process.
Raise visa type early with your recruiter
AbbVie sponsors E-3, TN, and H-1B1 visa in addition to the standard H-1B. If you're Australian, Canadian, or Chilean, flag your nationality in the first recruiter conversation. These visa types bypass the H-1B lottery and can significantly accelerate your start date.
Use Migrate Mate to filter open Healthcare roles by visa type
Not every open Healthcare position at AbbVie will proceed to sponsorship on the same timeline. Use Migrate Mate to browse current AbbVie Healthcare listings filtered by the visa types you're eligible for, so you're applying where sponsorship is actively supported.
Prepare for PERM timelines if Green Card is your goal
AbbVie supports EB-2 and EB-3 pathways for Healthcare professionals. PERM recruitment and DOL certification currently run 12 to 18 months before the I-140 petition stage. Raise permanent residency intent during the offer negotiation phase, not after you've started.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Healthcares?
Yes, AbbVie sponsors H-1B visas for qualifying Healthcare roles. Positions in clinical operations, regulatory affairs, pharmacovigilance, and medical affairs commonly meet USCIS's specialty occupation standard. AbbVie also sponsors H-1B1 visas for Chilean and Singaporean nationals and E-3 visas for Australians, both of which bypass the annual H-1B lottery.
How do I apply for Healthcare jobs at AbbVie?
Applications go through AbbVie's careers portal at abbvie.com/careers. Search by function, therapeutic area, or location. You can also browse open Healthcare roles at AbbVie filtered by visa type on Migrate Mate, which surfaces positions where sponsorship is actively supported. Tailor your resume to AbbVie's specific therapeutic focus areas before applying.
Which visa types does AbbVie commonly use for Healthcare roles?
AbbVie sponsors H-1B, H-1B1 visa, E-3, TN, F-1 OPT, F-1 CPT, J-1 visa, and Green Card pathways including EB-2 and EB-3. For Healthcare professionals, H-1B is the most common route for non-treaty nationals. Australians, Canadians, and Mexicans may qualify for E-3 or TN status, which offer faster timelines and no lottery exposure.
What qualifications does AbbVie expect for Healthcare roles with visa sponsorship?
Most Healthcare roles at AbbVie that qualify for sponsorship require at minimum a bachelor's degree in a directly related field, such as life sciences, pharmacy, nursing, or public health. Advanced degrees are common in regulatory affairs and medical science liaison positions. AbbVie's therapeutic areas include immunology, oncology, neuroscience, and aesthetics, so domain-specific experience strengthens candidacy considerably.
How long does the visa sponsorship process take for a Healthcare role at AbbVie?
Timeline depends on visa type. E-3 and TN approvals can move in two to four weeks from offer acceptance. H-1B cap-subject petitions follow USCIS's April lottery cycle, with an October 1 start date at the earliest. If AbbVie files for premium processing, USCIS adjudicates within 15 business days of receipt. Green Card pathways through PERM typically add 12 to 18 months before the I-140 stage.