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About the Role

Conceive and execute novel scientific research or development in Clinical Pharmacology to achieve project and CPPM goals. Generate new PK/PD proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques in the PK/PD field. Act as a lead PK scientist, critically evaluate advances, and integrate knowledge into research or development programs.

Responsibilities

• Contribute to clinical development by supporting Phase 1-4 studies including study design and clinical pharmacology strategy.
• Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports, relevant section of investigator brochures, common technical documents, white papers, and other similar documents.
• Conduct data analyses including non-compartmental analyses, modeling and simulation, and literature data analyses.
• Participate and present at various departmental and cross-functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, and Journal club.
• Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a unified clinical pharmacology position to clinical, CMC, and regulatory teams.
• Author scientific publications and present at scientific conferences.

Requirements

• PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field.
• Master’s Degree or equivalent education and typically 8+ years of experience.
• Bachelor’s Degree or equivalent education and typically 10+ years of experience.
• Excellent interpersonal skills.
• Ability to interact externally and internally and perform in a team setting.
• Demonstrates scientific acumen and has technical skills to perform the role.
• Persistent and resilient; finds the way to move good ideas forward.
• Uses mistakes, failure, and reflection as vehicles for learning and improvement.
• Delivers business results while also positioning AbbVie for long-term success.
• Connects unrelated concepts; generates original or unique ideas.
• Influences colleagues to achieve cross-functional alignment.

Skills

• PK
• PBPK
• PK-PD
• Pharmacometrics
• Systems pharmacology
• Drug metabolism/Transporters

Experience Level

• 0+ years of experience (PhD)
• 2+ years of experience (Pharm D)
• 8+ years of experience (Master's Degree)
• 10+ years of experience (Bachelor's Degree)

Education Level

• PhD
• Pharm D
• Master’s Degree
• Bachelor’s Degree

Salary/Compensations

• USD 109500 - USD 208500 - yearly

Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• Eligible to participate in our long-term incentive programs.

About the Company

• 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.

Equal Opportunity

• 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