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New · posted Nov 1

Bristol Myers Squibb · Pharmaceuticals

Patient Safety Intern Summer 2027

  • Princeton, NJ
  • On-site
  • Internship
  • Associate & Specialist
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EmploymentInternship
DeadlineCloses Nov 26, 2026

The role

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

The Patient Safety Intern will gain hands-on experience across multiple areas of pharmacovigilance and drug safety while supporting strategic initiatives that advance patient-centric, insights-driven safety capabilities. This internship offers a unique opportunity to work alongside experienced professionals, develop technical and business skills, and build a strong professional network within the biopharmaceutical industry.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

What you need

Required

  • Currently pursuing a Bachelor's, Master's, or Ph.D. degree in Data Science, Statistics, Mathematics, Life Sciences, Health Sciences, Public Health, Epidemiology, or a related field.
  • Strong written and verbal communication skills.
  • Proficiency in Microsoft Office applications, including Excel, PowerPoint, and Word.
  • Strong analytical and problem-solving skills.
  • Excellent organizational skills with strong attention to detail.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Demonstrated ability to work independently and collaboratively within diverse teams.

Preferrednice to have

  • Interest in healthcare, pharmaceuticals, life sciences, or patient safety.
  • Experience working with data analysis, visualization, or reporting tools.
  • Familiarity with digital technologies, artificial intelligence, or automation concepts.
  • Experience conducting research and synthesizing information from multiple sources.
  • Exposure to project management, process improvement, or operational excellence methodologies.

Core Competencies

  • Analytical thinking and problem solving
  • Data analysis and interpretation
  • Written and verbal communication
  • Attention to detail and quality
  • Project management and organization
  • Collaboration and teamwork
  • Learning agility and intellectual curiosity
  • Digital and AI mindset
  • Initiative and accountability
  • Commitment to patient-centric innovation

What you'll do

  • Support the development, editing, design, and formatting of internal and external communications, presentations, and reports.
  • Conduct research on emerging trends, technologies, and innovations related to safety data collection, analysis, evaluation, and communication to inform Patient Safety strategies.
  • Assist with data integrity reviews, reporting activities, and quality checks to support accurate and reliable safety data.
  • Generate, analyze, and present operational metrics and identify opportunities for process and reporting improvements.
  • Perform literature and data source searches to identify, evaluate, and summarize relevant scientific and safety information.
  • Support safety surveillance and signal detection activities across multiple therapeutic areas.
  • Assist with project management activities, proof-of-concept initiatives, and process improvement efforts.
  • Collaborate with cross-functional teams to support vendor management and risk management activities.
  • Organize project requirements and resources based on business priorities and ongoing portfolio activities.
  • Participate in networking events, mentorship opportunities, and professional development sessions offered through the internship program.

Pay and benefits

$43,680 – $93,600 a year

Employer provided

$21.00 – $45.00 an hour · yearly at 2,080 hours (40 a week)

How this compares

Compensation Overview

$21-$45/hour

Pay for this internship/co‑op position is provided in accordance with local market practices and applicable laws. Pay may be offered as an hourly rate and/or monthly stipend, or other locally compliant structure. Pay is determined based on objective factors such as academic level, relevant experience, skills, and work location.

Interns and co‑op participants may be eligible for limited benefits depending on program structure, work location, and local requirements. Eligibility and offerings are governed by applicable policies and employment regulations.

This is a temporary, time‑bound position intended for the duration of the internship or co‑op program and does not guarantee continued or permanent employment following program completion.

  • Mentorship opportunities

  • Networking events

  • Professional development sessions

  • Limited benefits for interns

Where you'll work

Princeton, NJOn-siteOpen in Maps (opens in a new tab)

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From the posting

About Bristol Myers Squibb

Why You Should Apply

This internship provides an opportunity to gain meaningful experience within a global biopharmaceutical company while contributing to initiatives that help ensure the safety of medicines and support better outcomes for patients worldwide. Interns will work closely with experienced professionals, receive mentorship, and develop skills that support future careers in healthcare, life sciences, analytics, and pharmaceutical development.

Bristol Myers Squibb company page · 46 open roles
Equal opportunity, accessibility and legal noticesBristol Myers Squibb's statements, word for word

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1607761 : Patient Safety Intern Summer 2027

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

This role's midpoint is 25% below the US median for Clinical Safety & Pharmacovigilance roles at this level.

This roleEmployer provided

$43,680 to $93,600 a year

Associate & Specialist roles in the US6 roles publishing pay

Middle half $77,750 to $102,500, median $92,000
Annual base pay
Annual base payLowMedianHigh
This role$43,680—$93,600
All US$77,750$92,000$102,500

This role: Bristol Myers Squibb'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 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 162 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Bristol Myers Squibb's own promotion track.

  1. This role

    Associate & Specialist

    Often: Associate, Pharmacovigilance Operations/Drug Safety · Clinical Safety Coordinator

    $92K median10 open
  2. Next step

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $172K median17 open
  3. Later

    Manager

    Often: Senior Manager, Clinical Quality Assurance · Clinical FSP Quality Manager

    $166K median30 open
  4. Later

    Director

    Often: Director · Senior Medical Director

    $264K median92 open
  5. Later

    VP & Executive

    Often: Head of Multiple Myeloma & AML, Oncology · Head of Patient-Facing Quality Assurance

    $347K median13 open

Skills DNA

What this role leans on

How many of the posting's 36 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

Lab testing and methods: 3 linesDocumentation and SOPs: 1 lineQuality systems and risk: 3 linesData and digital systems: 2 linesCollaboration and leadership: 10 linesLab testingDocumentationQuality systemsData systemsTeamwork
  • Collaboration and leadership10
  • Lab testing and methods3
  • Quality systems and risk3
  • Data and digital systems2
  • Documentation and SOPs1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

Bristol Myers Squibb on Regulatory Jobs

46
Open roles
45
Distinct roles
11
Locations

By discipline

  • Quality29 63%
  • Clinical9 20%
  • Regulatory8 17%

By level

  • Director13 28%
  • Associate & Specialist12 26%
  • Senior & Principal11 24%
See all 46 Bristol Myers Squibb roles

More roles at Bristol Myers Squibb

All 46 Bristol Myers Squibb roles

Similar Clinical Safety & Pharmacovigilance roles elsewhere

Patient Safety Intern Summer 2027 at Bristol Myers Squibb

Applications close November 26. $44K–$94K a year, employer provided.

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