Program Manager Jobs at AbbVie with Visa Sponsorship
Program Manager jobs at AbbVie span drug development, clinical operations, and commercial functions across therapeutic areas from immunology to oncology. The company has a consistent track record of sponsoring work visas for qualified program management professionals, making it a realistic target for international candidates.
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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 Clinical Operations Program Director is responsible to connect science and operations to bring clinical studies to life through the execution of one or more clinical research programs. The Clinical Operations Program Director serves as a strategic advocate for pipeline assets and provides operational reality to our scientific experiments via scientific expertise, strategic thinking, a global mindset and innovative solutions to address risks and challenges. The Clinical Operations Program Director also serves as an inspiring people leader responsible for developing a pipeline of talent for the Development Operations organization.
Responsibilities:
- Develop clinical operational strategy and ensure clinical research programs are executed with quality and efficiency, on-time, within budget, and to meet company objectives
- Translate asset strategy into operational execution by developing the clinical operations plan (or strategy) and connecting the science with the business, operations, patients and our customers
- Identify and evaluate risks and mitigations at program level to achieving the asset strategy
- Interacts with and influences all levels of management and cross-functional team members to achieve program objectives and represents Clinical Development Operations at senior leader cross functional meetings
- Reviews and provides clinical operations content to clinical and regulatory documents
- Manage overall external budget management across their portfolio (programs can be 20-200 million dollars)
- Responsible for bringing the best out of our talent, mentoring and supporting development to enable growth including direct management of study manager(s)
- Create an inclusive, innovative and learning environment where staff and studies/programs will succeed
- Execute clinical programs in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures)
- Strong communication and stakeholder management skills. Is comfortable with not having all the information yet able to drive activities and find solutions to deliver on the program
- Significant Work Activities - Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Qualifications
- Bachelor’s degree or equivalent is required, typically in nursing or scientific field. An Associate’s degree/R.N. or equivalent with relevant experience is acceptable
- Must have 12+ years of Pharma-related/clinical research related experience (and/or applicable work experience)
- Must have 8 years (and/or applicable work experience) in clinical research demonstrating a high level of core, technical and leadership competencies through setting and driving strategy
- Proven ability in leading a global team in the management and completion of multiple, complex clinical studies
- Ability to demonstrate successful coaching/mentoring and people management (remote management experience preferred)
- Expertise in Subject Matter and competent in application of standard business procedures (SOPs, ICH, Global Regulations, Ethics and Compliance)
- Integral participation in initiatives or advancement strategies for clinical operations
- Experience in successful study initiation through study completion/primary data analysis and in multiple phases of studies (Phase 1-3, 4)
- Must possess good 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
The Clinical Operations Program Director is responsible to connect science and operations to bring clinical studies to life through the execution of one or more clinical research programs. The Clinical Operations Program Director serves as a strategic advocate for pipeline assets and provides operational reality to our scientific experiments via scientific expertise, strategic thinking, a global mindset and innovative solutions to address risks and challenges. The Clinical Operations Program Director also serves as an inspiring people leader responsible for developing a pipeline of talent for the Development Operations organization.
Responsibilities:
- Develop clinical operational strategy and ensure clinical research programs are executed with quality and efficiency, on-time, within budget, and to meet company objectives
- Translate asset strategy into operational execution by developing the clinical operations plan (or strategy) and connecting the science with the business, operations, patients and our customers
- Identify and evaluate risks and mitigations at program level to achieving the asset strategy
- Interacts with and influences all levels of management and cross-functional team members to achieve program objectives and represents Clinical Development Operations at senior leader cross functional meetings
- Reviews and provides clinical operations content to clinical and regulatory documents
- Manage overall external budget management across their portfolio (programs can be 20-200 million dollars)
- Responsible for bringing the best out of our talent, mentoring and supporting development to enable growth including direct management of study manager(s)
- Create an inclusive, innovative and learning environment where staff and studies/programs will succeed
- Execute clinical programs in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures)
- Strong communication and stakeholder management skills. Is comfortable with not having all the information yet able to drive activities and find solutions to deliver on the program
- Significant Work Activities - Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Qualifications
- Bachelor’s degree or equivalent is required, typically in nursing or scientific field. An Associate’s degree/R.N. or equivalent with relevant experience is acceptable
- Must have 12+ years of Pharma-related/clinical research related experience (and/or applicable work experience)
- Must have 8 years (and/or applicable work experience) in clinical research demonstrating a high level of core, technical and leadership competencies through setting and driving strategy
- Proven ability in leading a global team in the management and completion of multiple, complex clinical studies
- Ability to demonstrate successful coaching/mentoring and people management (remote management experience preferred)
- Expertise in Subject Matter and competent in application of standard business procedures (SOPs, ICH, Global Regulations, Ethics and Compliance)
- Integral participation in initiatives or advancement strategies for clinical operations
- Experience in successful study initiation through study completion/primary data analysis and in multiple phases of studies (Phase 1-3, 4)
- Must possess good 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 Program Manager Jobs at AbbVie
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Get Access To All JobsTips for Finding Program Manager Jobs at AbbVie
Align your credentials to biopharma standards
AbbVie's Program Manager roles in clinical or regulatory functions often require PMP certification or an advanced degree in life sciences. Confirm your credentials map to the specific team you're targeting before applying.
Target therapeutic area teams strategically
AbbVie concentrates program management hiring around immunology, oncology, and neuroscience pipelines. Searching by therapeutic area rather than just job title surfaces roles where cross-functional coordination experience, not just project management, is the real differentiator.
Clarify visa type compatibility early
AbbVie sponsors multiple visa categories for Program Managers, including H-1B, E-3, TN, and F-1 OPT. Raise your visa type in the recruiter screen, not after an offer, so the right sponsorship pathway is confirmed before the process advances.
Understand the LCA filing requirement
Before AbbVie can petition USCIS for your H-1B, the company must file a Labor Condition Application with the DOL certifying your offered wage meets prevailing levels. Delays here can push your start date, so ask your recruiter about the LCA timeline during offer negotiation.
Use Migrate Mate to filter verified sponsoring roles
Program Manager openings at large biopharma companies aren't always tagged with sponsorship eligibility on general job boards. Use Migrate Mate to filter AbbVie listings to roles where visa sponsorship has been confirmed, saving time on applications that won't move forward.
Account for PERM timing if pursuing permanent residency
If you're targeting a Green Card through AbbVie's EB-2 or EB-3 pathway, PERM labor certification can take 12 to 18 months before USCIS even receives your I-140. Discuss the company's green card policy during the offer stage, not after you've started.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Program Managers?
Yes, AbbVie sponsors H-1B visas for Program Manager roles. Program management positions in drug development, clinical operations, and commercial functions typically qualify as specialty occupations under USCIS standards, requiring a bachelor's degree or higher in a relevant field. AbbVie handles the petition process through its legal team, and sponsorship is generally initiated after a formal offer is extended.
Which visa types does AbbVie commonly sponsor for Program Manager roles?
AbbVie sponsors several visa categories for Program Managers, including H-1B, H-1B1 visa, E-3 visa, TN visa, J-1 visa, and F-1 OPT and CPT. The right category depends on your nationality and current status. Australian citizens are eligible for E-3 visa, Canadian and Mexican nationals can pursue TN visa, and current F-1 students often start on OPT before transitioning to employer-sponsored status.
What qualifications does AbbVie expect for Program Manager roles?
Most Program Manager roles at AbbVie require a bachelor's degree in life sciences, engineering, business, or a related field, with several years of relevant program or project management experience. Roles tied to clinical development or regulatory affairs often prefer candidates with direct biopharma backgrounds. PMP certification strengthens applications for roles with cross-functional or enterprise-level scope.
How do I apply for Program Manager jobs at AbbVie?
You can search and apply for Program Manager roles directly through AbbVie's careers site or use Migrate Mate to browse verified AbbVie openings filtered by visa sponsorship eligibility. When applying, tailor your resume to the specific therapeutic area or function the role supports. After submitting, initial screening typically happens within two to three weeks for active requisitions.
How do I understand the timeline for H-1B sponsorship at AbbVie?
If you need cap-subject H-1B sponsorship, AbbVie must register you in USCIS's lottery in March for an October 1 start date. If selected, the petition window opens April 1. For candidates already on H-1B with another employer, AbbVie can file an H-1B transfer and you can start once USCIS issues a receipt notice, without waiting for October 1.