Medical Laboratory Scientist Jobs at AbbVie with Visa Sponsorship
Medical Laboratory Scientist jobs at AbbVie span pharmaceutical research and development operations, offering roles that sit at the intersection of clinical diagnostics and drug development. The company has a consistent track record of sponsoring work visas for this function, supporting candidates through both nonimmigrant and immigrant pathways.
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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 40+ Medical Laboratory Scientist Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Medical Laboratory Scientist Jobs at AbbVie.
Get Access To All JobsTips for Finding Medical Laboratory Scientist Jobs at AbbVie
Align your credentials to CLIA-regulated lab standards
AbbVie's lab roles often require ASCP or AMT certification alongside your degree. Confirm your credentials meet U.S. Clinical Laboratory Improvement Amendments standards before applying, since pharmaceutical employers treat certification as a hard filter, not a preference.
Target AbbVie's discovery and translational research sites
AbbVie concentrates Medical Laboratory Scientist hiring at its North Chicago headquarters and key R&D campuses. Filtering your search by these locations surfaces roles with the highest likelihood of active visa sponsorship, rather than administrative or commercial sites with fewer lab positions.
Browse open Medical Laboratory Scientist roles on Migrate Mate
Migrate Mate filters AbbVie's open Medical Laboratory Scientist positions by visa type, so you can confirm which roles are actively sponsoring before you invest time in the application process. It removes the guesswork about which postings are relevant to your situation.
Understand how AbbVie structures H-1B specialty occupation evidence
For Medical Laboratory Scientist roles, USCIS requires proof the position normally requires a directly related bachelor's degree or higher. Highlight in your application materials that your degree field, such as clinical laboratory science or medical technology, corresponds specifically to the advertised role.
Start OPT or CPT conversations with your recruiter early
AbbVie sponsors F-1 OPT and CPT for laboratory roles, but hiring timelines in pharma R&D rarely flex around academic calendars. Contact the recruiter in your first conversation to align your OPT start date with the team's onboarding window and avoid a gap in authorization.
Prepare for PERM labor certification if targeting a Green Card
AbbVie supports EB-2 and EB-3 pathways for qualifying Medical Laboratory Scientists, but DOL's PERM process requires the employer to advertise the role under strict conditions first. Ask your hiring manager about the internal timeline for initiating PERM after you clear your first year of employment.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Medical Laboratory Scientists?
Yes, AbbVie sponsors H-1B visas for Medical Laboratory Scientists. The role qualifies as a specialty occupation under USCIS standards because it requires a directly related bachelor's degree in clinical laboratory science, medical technology, or a closely aligned field. AbbVie also sponsors the H-1B1 visa for Chilean and Singaporean nationals and the E-3 visa for Australian citizens, giving candidates multiple H-1B visa-family options depending on nationality.
How do I apply for Medical Laboratory Scientist jobs at AbbVie?
Apply directly through AbbVie's careers portal by searching for Medical Laboratory Scientist or related titles filtered by location. You can also use Migrate Mate to browse AbbVie's open Medical Laboratory Scientist roles filtered by visa sponsorship type, which makes it easier to identify which postings are relevant before submitting your application. Tailor your resume to highlight ASCP or AMT certification and any experience in pharmaceutical or clinical trial laboratory environments.
Which visa types does AbbVie commonly sponsor for Medical Laboratory Scientists?
AbbVie sponsors a broad range of visa types for this role, including H-1B, H-1B1 visa, E-3, TN, J-1 visa, and F-1 OPT and CPT for students and recent graduates. For candidates seeking permanent residence, AbbVie supports EB-2 and EB-3 Green Card pathways. The TN visa is available to Canadian and Mexican nationals whose occupation category aligns with the role's qualifying duties under USMCA.
What qualifications does AbbVie expect for Medical Laboratory Scientist roles?
AbbVie typically expects a bachelor's degree in clinical laboratory science, medical technology, or a closely related biomedical field, along with current ASCP Board of Certification or equivalent credentialing. Roles in pharmaceutical R&D often require familiarity with GMP or GLP environments, and positions supporting clinical trials may require experience with CAP-accredited or CLIA-certified workflows. Advanced degree holders with a research focus can qualify for senior-level positions.
How long does the visa sponsorship process take when joining AbbVie as a Medical Laboratory Scientist?
Timeline depends on the visa type. H-1B standard processing takes three to six months after USCIS receives the petition on April 1, with premium processing available for a faster decision. E-3 and TN visas can move significantly quicker, often within weeks at a consulate or port of entry. For Green Card pathways through PERM, the full process from labor certification to I-140 approval typically spans one to two years before priority date considerations apply.