Clinical Director Jobs at AbbVie with Visa Sponsorship
Clinical Director jobs at AbbVie span therapeutic areas including immunology, oncology, and neuroscience, with roles that sit at the intersection of clinical strategy and cross-functional leadership. AbbVie has an established track record of sponsoring work visas for this function, making it a realistic target for international candidates.
Find Clinical Director Jobs at AbbVieOverview
Showing 5 of 14+ Clinical Director Jobs at AbbVie
See all Clinical Director Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Director Jobs at AbbVie.
Get Access To All JobsCompany 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
Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management, regulatory agencies, and external peers. Supports strategic planning for drug development activities and projects to achieve departmental strategies, goals, and objectives. Utilizes scientific expertise to provide appropriate interpretation of data and relates implications of results to management. Serves as liaison to other departments/divisions for any study/project needs. Understands linkages across businesses and understands the impact of business decisions and solutions. May lead teams within Clinical Pharmacology and Pharmacometrics and accountable for effective performance of the teams.
Responsibilities
- Leads Clinical Pharmacology/PK/PD activities and multiple major projects. Assists R&D senior management in the selection of action plans that best meets drug development business objectives.
- Identifies issues and help with issue resolution. Conducts risk assessments and assists in development of contingency plans. Assures project remains in alignment with strategic objectives.
- Provides overall timelines to assess portfolio opportunities. Negotiates with other functional areas on project outcomes and deliverables to meet conflicting demands (time, cost, quality/performance).
- Provides scientific and strategic consultation to R&D, Regulatory, and all levels of management on critical decisions and development plans.
- Responsible for evaluating technical, scientific aspects of all AbbVie projects along with CLINICAL PHARMACOLOGY management. Reviews clinical protocols and scientific reports for regulatory filings and anticipates regulatory questions. Leads CLINICAL PHARMACOLOGY regulatory documents writing, submission and response to Regulatory agency comments.
- Independently conducts due diligence assessments, summarizes results and represents CLINICAL PHARMACOLOGY on business development teams.
- Identifies and develops process improvement initiatives and reviews recommendations with management for approval and sponsorship.
- Contribute to development of departmental goals. Influences strategic PK/PD decisions for the department.
- Performs functions and responsibilities with the highest regard for quality and timeliness. Maintains up-to-date knowledge of PK/PD data analysis, modeling and simulation methods and software.
- May manage personnel including development, mentoring, and effective delegation.
Qualifications
- PhD with typically 7+ years of experience or Pharm D with typically 9+ years of experience in a relevant field, MS or equivalent education with typically 15+ years of experience; BS or equivalent education and typically 17+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
- Excellent interpersonal skills
- Knowledge and experience in multiple therapeutic and/or functional areas
- Experience across range of development phases
- Knowledge of AbbVie and Pharma drug development processes
- Must have demonstrated leadership competencies in PK/PD, Biopharmaceutics, and Pharmacometric activities from planning, implementation through completion across multiple projects
- Scientific project leadership or related experience
- Project management skills such as scope management, progress tracking/driving as well as time management
- Participates in initiatives and advancement of CLINICAL PHARMACOLOGY
Key Leadership Competencies:
- Knows the business and the cross-functional contributions needed to deliver results
- Persistent and resilient finds the way to move good ideas forward
- Acts respectfully yet courageously
- Connects unrelated concepts, generates original or unique ideas
- Influences colleagues to achieve cross-functional alignment
- Communicates openly and honestly with all colleagues
- Manages conflict and difficult conversations in a constructive transparent way
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
Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management, regulatory agencies, and external peers. Supports strategic planning for drug development activities and projects to achieve departmental strategies, goals, and objectives. Utilizes scientific expertise to provide appropriate interpretation of data and relates implications of results to management. Serves as liaison to other departments/divisions for any study/project needs. Understands linkages across businesses and understands the impact of business decisions and solutions. May lead teams within Clinical Pharmacology and Pharmacometrics and accountable for effective performance of the teams.
Responsibilities
- Leads Clinical Pharmacology/PK/PD activities and multiple major projects. Assists R&D senior management in the selection of action plans that best meets drug development business objectives.
- Identifies issues and help with issue resolution. Conducts risk assessments and assists in development of contingency plans. Assures project remains in alignment with strategic objectives.
- Provides overall timelines to assess portfolio opportunities. Negotiates with other functional areas on project outcomes and deliverables to meet conflicting demands (time, cost, quality/performance).
- Provides scientific and strategic consultation to R&D, Regulatory, and all levels of management on critical decisions and development plans.
- Responsible for evaluating technical, scientific aspects of all AbbVie projects along with CLINICAL PHARMACOLOGY management. Reviews clinical protocols and scientific reports for regulatory filings and anticipates regulatory questions. Leads CLINICAL PHARMACOLOGY regulatory documents writing, submission and response to Regulatory agency comments.
- Independently conducts due diligence assessments, summarizes results and represents CLINICAL PHARMACOLOGY on business development teams.
- Identifies and develops process improvement initiatives and reviews recommendations with management for approval and sponsorship.
- Contribute to development of departmental goals. Influences strategic PK/PD decisions for the department.
- Performs functions and responsibilities with the highest regard for quality and timeliness. Maintains up-to-date knowledge of PK/PD data analysis, modeling and simulation methods and software.
- May manage personnel including development, mentoring, and effective delegation.
Qualifications
- PhD with typically 7+ years of experience or Pharm D with typically 9+ years of experience in a relevant field, MS or equivalent education with typically 15+ years of experience; BS or equivalent education and typically 17+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
- Excellent interpersonal skills
- Knowledge and experience in multiple therapeutic and/or functional areas
- Experience across range of development phases
- Knowledge of AbbVie and Pharma drug development processes
- Must have demonstrated leadership competencies in PK/PD, Biopharmaceutics, and Pharmacometric activities from planning, implementation through completion across multiple projects
- Scientific project leadership or related experience
- Project management skills such as scope management, progress tracking/driving as well as time management
- Participates in initiatives and advancement of CLINICAL PHARMACOLOGY
Key Leadership Competencies:
- Knows the business and the cross-functional contributions needed to deliver results
- Persistent and resilient finds the way to move good ideas forward
- Acts respectfully yet courageously
- Connects unrelated concepts, generates original or unique ideas
- Influences colleagues to achieve cross-functional alignment
- Communicates openly and honestly with all colleagues
- Manages conflict and difficult conversations in a constructive transparent way
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 Director Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Director Jobs at AbbVie.
Get Access To All JobsTips for Finding Clinical Director Jobs at AbbVie
Align your credentials to AbbVie's therapeutic focus
AbbVie's Clinical Director roles cluster around immunology, oncology, and aesthetics. Frame your CV around experience in these areas specifically, because a generalist clinical background will get screened out before sponsorship conversations even begin.
Confirm your degree field supports specialty occupation classification
Clinical Director petitions must satisfy USCIS specialty occupation requirements. A medical degree or graduate-level clinical science credential is typically expected. If your degree is in a tangentially related field, gather documentation showing it directly applies to the posted role.
Target AbbVie's internal medicine affairs and clinical development teams
AbbVie recruits Clinical Directors primarily through its Medical Affairs and Clinical Development organizations. Applications routed through these business units reach hiring managers already familiar with sponsorship workflows, which shortens the internal approval process significantly.
Understand which visa pathway fits your citizenship
AbbVie sponsors H-1B, E-3, TN, and H-1B1 visas for this role. Australian citizens can use the E-3 to sidestep the H-1B lottery entirely. Canadian and Mexican nationals on the TN pathway face no USCIS petition at all, which cuts filing time substantially.
Negotiate your start date around DOL and USCIS filing timelines
For H-1B transfers or cap-exempt filings, USCIS processing runs six to eight months without premium processing. Build that into offer negotiations. Requesting a start date that doesn't account for filing timelines puts your offer at risk before it even clears HR.
Use Migrate Mate to find open Clinical Director roles at AbbVie
AbbVie's sponsorship-eligible Clinical Director openings are filterable by visa type on Migrate Mate. Search before roles close, because clinical leadership postings at large pharmaceutical companies fill quickly and are rarely reposted at the same seniority level.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Clinical Directors?
Yes, AbbVie sponsors H-1B visas for Clinical Director roles. The company works with immigration counsel to file both cap-subject and cap-exempt petitions depending on the candidate's situation. If you're already in H-1B status with another employer, AbbVie can file an H-1B transfer, which isn't subject to the annual lottery and can proceed year-round.
How do I apply for Clinical Director jobs at AbbVie?
Applications go through AbbVie's careers portal at abbvie.com/careers. Search by function using terms like 'Clinical Director,' 'Medical Affairs Director,' or the specific therapeutic area you're targeting. You can also find sponsorship-eligible Clinical Director openings filtered by visa type on Migrate Mate, which helps you identify roles before they're filled.
Which visa types does AbbVie commonly use for Clinical Director positions?
AbbVie sponsors H-1B, H-1B1 visa, E-3 visa, TN visa, and J-1 visas for Clinical Directors, and also supports Green Card pathways including EB-2 and EB-3. For long-term hires, AbbVie typically initiates PERM labor certification through the DOL after the initial visa period, particularly for candidates intending to pursue permanent residence.
What qualifications does AbbVie expect for a Clinical Director role?
AbbVie typically requires an advanced degree, usually an MD, PharmD, or PhD in a clinical or life sciences discipline, along with substantive experience in clinical development or medical affairs within the pharmaceutical or biotechnology sector. Therapeutic area expertise in immunology, oncology, or neuroscience is frequently listed as a requirement rather than a preference for Clinical Director-level postings.
How do I time my application given AbbVie's visa filing process?
For H-1B cap-subject cases, USCIS registration opens in March for an October 1 start date. If you miss the lottery, AbbVie can file under cap-exempt status if you've previously held H-1B status. For E-3 and TN visas, there's no lottery and no annual cap, so timing is driven by how quickly AbbVie completes its internal offer and legal review process, which typically runs four to eight weeks.