2027 Summer Intern Pharmacovigilance Scientist Swiftwater PA

Sanofi•Swiftwater, PA

1d•Onsite

About The Position

Sanofi is seeking a highly motivated summer intern to join its Pharmacovigilance Scientist team in Swiftwater, Pennsylvania. The intern will gain experience with clinical development and marketed products and learn how pharmacovigilance (PV) supports products throughout their lifecycle. The role involves evaluating and communicating safety data, collaborating with internal teams and external partners or authorities, and learning about PV functions and key organizational stakeholders. The intern will also develop AI-driven approaches to PV activities, including signal detection, safety data analysis, and risk assessment, while maintaining regulatory compliance. The internship lasts 8–12 weeks. The intern must be able to relocate to the office location and work 40 hours per week, Monday through Friday, for the full duration of the internship. The stated salary range is $32.00–$35.00 per hour, with compensation determined based on demonstrated experience.

Requirements

Currently pursuing a Doctorate of Pharmacy (PharmD) and entering the summer after the first (P1) or second (P2) professional year.
Must be permanently authorized to work in the U.S. and not require employment visa sponsorship at application or in the future.
Must remain enrolled in an accredited college or university throughout the internship.
Must be able to relocate to the office location and work 40 hours per week, Monday through Friday, for the full internship duration.

Nice To Haves

Proficiency in Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook, for data compilation, analysis, and presentation.
Experience reviewing, organizing, or interpreting data sets through coursework, research projects, or prior work experience.
Exposure to clinical development, regulatory affairs, or FDA regulations through coursework, internships, or pharmacy school rotations.
Interest in or exposure to AI, machine learning, or data science applications in healthcare or pharmaceutical settings.
Strong written and verbal communication skills and ability to present complex information clearly to cross-functional audiences.
Self-motivation and demonstrated ability to work independently, manage multiple priorities, and meet deadlines with minimal supervision.

Responsibilities

Critically evaluate, interpret, synthesize, and present safety data clearly and concisely through written and verbal communication.
Gain experience with clinical development and marketed products to understand the role of pharmacovigilance throughout the product lifecycle.
Lead, engage, coordinate, and collaborate with internal teams and external partners or authorities.
Understand the roles of other functional areas within pharmacovigilance and key organizational stakeholders.
Demonstrate knowledge of global legislation related to safety and benefit-risk assessment and management.
Develop and implement innovative AI-driven solutions in pharmacovigilance activities to enhance signal detection, safety data analysis, and risk assessment while maintaining regulatory compliance.
Independently prioritize, plan, and manage multiple ongoing projects and timelines.