New · posted Nov 4
Sanofi · Pharmaceuticals
2027 Summer Intern Pharmacovigilance Scientist
- Swiftwater, PA
- On-site
- Internship
- Associate & Specialist
The role
Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. We are seeking a highly motivated Summer Intern to join our Pharmacovigilance Scientist team.
Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you’ll be empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams.
What you need
Basic Qualifications
Currently pursuing a Doctorate of Pharmacy (PharmD) in the summer after your first (P1) or second (P2) professional year.
Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the Internal requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.
Must be enrolled in an accredited college or university throughout the duration of the co-op/internship.
Must be able to relocate to the office location and work 40hrs/week, Monday to Friday for the full duration of the co-op/internship.
Preferred Qualificationsnice to have
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, 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 with ability to present complex information clearly to cross-functional audiences
- Self-motivated with demonstrated ability to work independently, manage multiple priorities, and meet deadlines with minimal supervision
What you'll do
Critically evaluate, interpret, synthesize, and present safety data in a clear and concise manner through written and verbal communication
Obtain experience with clinical development and marketed products to further understand the role of PV throughout the product lifecycle
Lead, engage, coordinate, and collaborate cross functionally with both internal teams and external partners/authorities
Understand the roles of other functional areas within PV and key players within the organization
Demonstrate knowledge of global legislation in safety and benefit-risk assessment/management
Develop and implement innovative AI-driven solutions in PV activities to enhance signal detection, safety data analysis, and risk assessment while maintaining regulatory compliance
Be self-motivated; able to independently prioritize, plan, and manage multiple ongoing projects and timelines
Pay and benefits
The salary range for this position is $32.00 - 35.00 USD hourly. All compensation will be determined commensurate with demonstrated experience.
Why Choose Us
Bring the miracles of science to life alongside a supportive, future focused team.
Stretch your skills through apprenticeships, internships, graduate programs, and international experiences that grow with you.
Learn from inspiring mentors and collaborative teams while contributing to real projects that shape the future of healthcare.
Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve.
Where you'll work
Swiftwater, PAOn-siteOpen in Maps (opens in a new tab)
More jobs in Swiftwater, PAWorking conditions
Job Title: 2027 Summer Intern Pharmacovigilance Scientist
Grade: Intern
Location: Swiftwater, PA
Duration: 8 - 12 Weeks
From the posting
About Sanofi
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
Equal opportunity, accessibility and legal noticesSanofi's statements, word for word
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here
Job intelligence
The context around this role
Live data · November 4, 2026
Salary intelligence
How the pay compares
This role's midpoint is 18% below the US median for Clinical Safety & Pharmacovigilance roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US7 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $66,560 | — | $66,560 |
| All US (middle half) | $73,250 | $81,500 | $102,500 |
This role: Sanofi's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Safety & Pharmacovigilance
The general path across 160 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Sanofi's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 19 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership5
- GMP and compliance2
- Quality systems and risk2
- Clinical trial conduct2
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Safety & Pharmacovigilance work in pharmaceuticals, each linked to the agency or standards body that publishes it.
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- FDAFDA good pharmacovigilance practices(official source, opens in a new tab)Good Pharmacovigilance Practices and Pharmacoepidemiologic Assessment
- FDAFDA FAERS(official source, opens in a new tab)The FDA Adverse Event Reporting System for drugs and biologics
- EMAEU Good Pharmacovigilance Practices (GVP)(official source, opens in a new tab)EMA's modules for pharmacovigilance systems, signals and periodic reports
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
- FDAFDA REMS(official source, opens in a new tab)Risk Evaluation and Mitigation Strategies for drugs with serious safety concerns
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- EUDirective 2001/83/EC(official source, opens in a new tab)The EU code for medicinal products for human use: authorization, labeling, pharmacovigilance
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 201(official source, opens in a new tab)FDA labeling requirements for drugs, including prescribing information
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- Health CanadaCanada Food and Drug Regulations(official source, opens in a new tab)Health Canada's regulations for drugs, including GMP (Part C, Division 2)
- MHRAUK MHRA(official source, opens in a new tab)The UK regulator of medicines and medical devices, including UKCA marking
- PMDAJapan PMDA(official source, opens in a new tab)Japan's Pharmaceuticals and Medical Devices Agency
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Sanofi on Regulatory Jobs
- 25
- Open roles
- 19
- Distinct roles
- 6
- Locations
By discipline
- Quality14 56%
- Regulatory6 24%
- Clinical5 20%
By level
- Senior & Principal9 36%
- Director5 20%
- Manager4 16%
More roles at Sanofi
- View role
Senior Clinical Research Director
Cambridge, MA · HybridDirectorPharmaceuticals$236K–$394K
- View role
Senior Clinical Research Director
Cambridge, MA · HybridDirectorPharmaceuticals$236K–$394K
- View role
Associate Clinical Research Director
Cambridge, MADirectorPharmaceuticals$173K–$249K
- View role
Senior Clinical Research Director
Cambridge, MA · HybridDirectorPharmaceuticals$236K–$394K
Similar Clinical Safety & Pharmacovigilance roles elsewhere
- View role
Patient Safety Associate I (Drug Safety Associate I)
ParexelRemote, USAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
Patient Safety Intern Summer 2027
Bristol Myers SquibbPrinceton, NJAssociate & SpecialistPharmaceuticals$44K–$94K
- View role
Specialist I, Patient Safety and Pharmacovigilance Operations
Corcept TherapeuticsRedwood City, CAAssociate & SpecialistPharmaceuticals$66K–$87K
- View role
Clinical Sciences Partnership COE Coordinator
AbbVieNorth Chicago, ILAssociate & SpecialistPharmaceuticals$59K–$104K
2027 Summer Intern Pharmacovigilance Scientist at Sanofi
Applications close November 9. $67K a year, employer provided.