Clinical Laboratory Scientist Jobs at AbbVie with Visa Sponsorship
Clinical Laboratory Scientist jobs at AbbVie span pharmaceutical research and manufacturing operations, supporting drug development and quality assurance workflows. The company has a consistent track record of sponsoring work visas for this function, making it a viable target if you're pursuing H-1B visa, E-3 visa, or F-1 OPT pathways in biotech.
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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
Purpose:
Oversees the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy.
Responsibilities:
- Manages the design and implementation of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and AbbVie study staff.
- Has overall responsibility for oversight of clinical studies, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned.
- Responsible for design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents.
- May oversee the work of Medical Directors and/or Scientific Directors, and of Clinical Scientists working on the same or related programs.
- Provides in-house clinical expertise for the molecule and disease, coordinating appropriate scientific and medical activities with internal stakeholders as they relate to ongoing clinical projects. May participate in due diligence or other business development activity. As required by program needs, contributes in partnership with Discovery colleagues to design and implementation of translational strategies.
- May serve on or chair a Clinical Strategy Team (CST), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches. In the role of CST Chair, responsibilities may include supervision of matrix team members and serving as Clinical Research representative to lend clinical development and medical expertise to an Asset Development Team (ADT), ADT Leadership Board (ALB).
- Acts as a clinical interface and actively solicits opinion leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
- Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area.
- Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
- Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Qualifications
- Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program strongly preferred. Completion of a subspecialty fellowship is desirable.
- At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
- Ability to run a clinical research program of moderate complexity with minimal supervision.
- Ability to perform and bring out the best in others on a cross-functional global team.
- Ability to interact externally and internally to support a global scientific and business strategy.
- Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
- Must possess excellent oral and written English communication 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 long-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
Purpose:
Oversees the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy.
Responsibilities:
- Manages the design and implementation of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and AbbVie study staff.
- Has overall responsibility for oversight of clinical studies, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned.
- Responsible for design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents.
- May oversee the work of Medical Directors and/or Scientific Directors, and of Clinical Scientists working on the same or related programs.
- Provides in-house clinical expertise for the molecule and disease, coordinating appropriate scientific and medical activities with internal stakeholders as they relate to ongoing clinical projects. May participate in due diligence or other business development activity. As required by program needs, contributes in partnership with Discovery colleagues to design and implementation of translational strategies.
- May serve on or chair a Clinical Strategy Team (CST), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches. In the role of CST Chair, responsibilities may include supervision of matrix team members and serving as Clinical Research representative to lend clinical development and medical expertise to an Asset Development Team (ADT), ADT Leadership Board (ALB).
- Acts as a clinical interface and actively solicits opinion leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
- Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area.
- Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
- Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Qualifications
- Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program strongly preferred. Completion of a subspecialty fellowship is desirable.
- At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
- Ability to run a clinical research program of moderate complexity with minimal supervision.
- Ability to perform and bring out the best in others on a cross-functional global team.
- Ability to interact externally and internally to support a global scientific and business strategy.
- Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
- Must possess excellent oral and written English communication 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 long-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 Clinical Laboratory Scientist Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Laboratory Scientist Jobs at AbbVie.
Get Access To All JobsTips for Finding Clinical Laboratory Scientist Jobs at AbbVie
Align Your Credentials With CLIA Requirements
AbbVie's lab roles typically require ASCP or equivalent certification. Confirm your credentials meet CLIA-defined standards before applying, since hiring managers in pharmaceutical QC environments screen for this before moving candidates to the sponsorship conversation.
Target Roles Tied to Drug Manufacturing Sites
AbbVie's Clinical Laboratory Scientist openings concentrate around its North Chicago headquarters and manufacturing facilities. Applying to site-specific postings rather than general research roles improves your odds of landing in a team that regularly sponsors visas for this function.
Use Migrate Mate to Surface Active Openings
AbbVie's sponsorship-eligible lab roles don't always stay posted long. Use Migrate Mate to filter specifically for Clinical Laboratory Scientist positions at AbbVie that support visa sponsorship, so you're applying to active listings before they close.
Clarify OPT Cap-Gap Coverage Before Your Start Date
If you're on F-1 OPT and receive an AbbVie offer, confirm your H-1B petition will be filed before your OPT expires. USCIS cap-gap protection extends your authorization automatically if the petition is filed on time, but you need to track your own expiration dates carefully.
Expect a PERM-Based Timeline for Permanent Residency
AbbVie sponsors EB-2 and EB-3 Green Cards for lab scientist roles, which means DOL's PERM labor certification is typically the first step. That process can take one to two years before an I-140 petition is filed, so factor that into your long-term planning.
Address Your Nonimmigrant Intent Directly in the Interview
For E-3 and H-1B1 visa candidates, AbbVie's HR teams want to understand your authorization timeline upfront. Come prepared to explain your current status, expiration date, and which petition type applies, so the offer stage doesn't stall on visa logistics.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Clinical Laboratory Scientists?
Yes, AbbVie sponsors H-1B visas for Clinical Laboratory Scientists. The company participates in the annual H-1B cap lottery for new applicants and also files for cap-exempt extensions and transfers. Clinical Laboratory Scientist roles typically qualify as specialty occupations under USCIS criteria, given the degree and certification requirements attached to these positions.
How do I apply for Clinical Laboratory Scientist jobs at AbbVie?
You can apply directly through AbbVie's careers portal or find sponsorship-eligible openings through Migrate Mate, which filters specifically for visa-sponsored roles. When applying, tailor your resume to highlight relevant laboratory certifications such as ASCP, your experience with regulated environments, and any pharmaceutical or biotech lab background, since AbbVie prioritizes candidates with industry-specific QC or QA exposure.
Which visa types does AbbVie commonly use for Clinical Laboratory Scientists?
AbbVie sponsors a range of visa types for Clinical Laboratory Scientists, including H-1B, E-3 for Australian nationals, TN visa for Canadian and Mexican professionals, H-1B1 visa for Chilean and Singaporean nationals, and F-1 OPT and CPT for students. For permanent residency, AbbVie supports EB-2 and EB-3 Green Card pathways through the DOL PERM labor certification process.
What qualifications does AbbVie expect for Clinical Laboratory Scientist roles?
AbbVie typically requires a bachelor's degree in clinical laboratory science, medical technology, or a closely related field, along with ASCP certification or an equivalent credential. Experience in a regulated pharmaceutical or clinical environment is a strong differentiator. Familiarity with GMP or GLP standards is frequently listed in postings tied to AbbVie's manufacturing and quality control sites.
How long does the visa sponsorship process take if I receive an offer from AbbVie?
Timeline depends on visa type. H-1B petitions are filed once per year for an October 1 start date, so timing your offer relative to the March registration window matters. E-3 and TN visas move faster, often within a few weeks of an approved Labor Condition Application from DOL. Green Card sponsorship through PERM typically adds one to two years before the I-140 stage begins.