2026 Global Patient Safety, Oncology TA Intern (PhD)

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Global Patient Safety, Oncology TA Intern Overview  

Envision spending your summer working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie Interns. 

The Global Patient Safety, Oncology Therapeutic Area (TA) Intern will spend your summer engaged with energetic colleagues and inspirational leaders, gaining world-class experience within one of the most dynamic organizations in the pharmaceutical industry. The intern will support the enhancement of clinical safety insights by leveraging reverse translatability to improve non-clinical capabilities (e.g. complex in vitro models (CIVM) or new approach methodologies (NAMs). Additionally, the intern will learn GPS processes and deliverables relevant to clinical development and patient safety. 

The Global Patient Safety (GPS) organization works collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand, and communicate the safety profile of AbbVie products to protect patients worldwide. The team plays a critical role in evaluating safety data relevant to AbbVie for both pharmaceutical and medical device products.  

The team is a high-profile and high-impact group of physicians and other health care professionals who work in close collaboration with a broad range of cross-functional colleagues. The team works collaboratively to provide product data analysis, signal monitoring, and product insights so that together as a team, the Product Safety Team (PST) can implement appropriate actions to ensure patient safety. 

As a member of the team, you are at the forefront of working with leaders to identify critical priorities and drive high-value projects that make an impact on the safety of our patients. 

Key Responsibilities Include: 

• Collaborate with PST Leads and Preclinical Safety colleagues to identify gaps in current complex in vitro models (CIVM) and new approach methodologies (NAMs) capabilities as they relate to ongoing and potential clinical safety challenges. 

• Partner with teams across Discovery, Development Biological Sciences, and Genomics, as well as external collaborators when appropriate, to enhance CIVM/NAMs and improve their utility in addressing clinical safety questions. 

• Leverage reverse translatability to inform the development and refinement of non-clinical models based on clinical safety insights. 

• Assist in the effective utilization and organization of data related to model capabilities and enhancements. 

• Contribute to the overall goals of bridging gaps between non-clinical and clinical safety, helping to inform AbbVie’s R&D pipeline and clinical safety decision-making. 

• Prepare summaries or presentations of findings and recommendations for internal stakeholders, demonstrating progress and impact on model capabilities. 

Minimum Qualifications  

• Currently enrolled in university, pursuing a PhD in biology, chemistry or related scientific discipline, or a programming or computational skill that is related to a scientific discipline, or other related degree. 

• Must be enrolled in university for at least one semester following the internship.  

• Experience with in vitro models (CIVM) and new approach methodologies (NAMs) capabilities 

• Ability to summarize complex information.

• Strong verbal and written communication skills.

• Takes initiative and always looks for improvement opportunities.

Preferred Qualifications 

• Expected graduation date between December 2026 – June 2027. 

Benefits and Amenities  

• Competitive pay  

• Relocation support for eligible students 

• Opportunities for professional development and mentorship 

• Access to dynamic project experiences within a world-class pharmaceutical organization

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

Benefits and Amenities:​

• Competitive pay​

• Relocation support for eligible students​

• Select wellness benefits and paid holiday / sick time ​

• 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.​

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. 

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