Future Opportunities - Join Our Talent Pipeline for Safety Data Scientist

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 and LinkedIn. 

Thank you for considering a future opportunity with our company! We are not currently hiring for this specific role, but we would love to connect with talented individuals who are interested in potential future positions. By joining our talent pipeline, you will be the first to be notified when suitable opportunities arise. 

In this talent pipeline requisition, we are not actively recruiting for this position at the moment. However, we are building a network of exceptional individuals who possess the skills and experience required for future openings. By submitting your application to this requisition, you will be added to our talent pipeline and considered for future opportunities. 

Join us as a Safety Data Scientist and contribute to the safety and well-being of patients in the development of life-saving medications. In this role, you will conduct standard surveillance activities for a product's life cycle, reviewing safety data from clinical trials, databases, and literature. Collaborating with safety and clinical teams, you will analyze data from multiple sources to support signal assessments and regulatory requests. Your medical judgment will be crucial in determining the impact of safety issues on the benefit-risk profile of the compound/product. You will communicate your findings to inform necessary risk minimization activities, including label changes. Minimum qualifications include a degree in a Health Sciences field and knowledge of the drug development process. Join us and make a difference in patient safety.

The Safety Data Scientist is responsible for conducting standard surveillance activities for a product's life cycle, including the review of safety data from clinical trials, safety databases, and the literature. They collaborate with safety and clinical teams to develop strategies and approaches for signal assessments and regulatory requests by analyzing data from multiple sources. The Safety Data Scientist also contributes to ad hoc regulatory safety requests and utilizes medical judgment to determine the impact of identified safety issues on the compound/product's benefit-risk profile. They communicate their findings to product teams and leadership to inform necessary risk minimization activities, including label changes.

Responsibilities:

• Conduct standard surveillance activities for one or more assigned compounds and products throughout their life cycle.
• Collaborate with safety and clinical teams to develop strategies and approaches for signal assessments and regulatory requests.
• Analyze data from multiple sources to support signal assessment and contribute to ad hoc regulatory safety requests under supervision.
• Utilize medical judgment to determine the impact of identified safety issues on the compound/product's benefit-risk profile.
• Communicate findings of surveillance activities and safety assessments to product teams and leadership to inform necessary risk minimization activities, including label changes.

• Degree in a Health Sciences field (e.g., Pharmacy, Epidemiology, Nursing).
  • Bachelor's degree with 2 years of clinical/pharma or safety work experience.
  • Master's or doctorate degree with 1-2 years of clinical/pharma or safety work experience (e.g., MPH, PharmD, PhD, or Masters in a Health Science).
• Knowledge of the drug development process, including conducting clinical trials, scientific strategy and operations management for the planning, execution, and reporting of clinical development programs, and regulatory requirements for submission, product launch, and post-marketing support.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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