Boehringer Ingelheim Posted October 7, 2026

University Intern - Patient Safety & Pharmacovigilance (Bracknell Forest, United Kingdom, Aberdeen City)

Bracknell Forest, United Kingdom Type not listed
Pharmacovigilance Intern/Fellow/Postdoc
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Boehringer Ingelheim is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Number of opportunities: 1

Salary: £26,000 (Not flexible)  

Closing date: 26/10/2026

This is a 12-month paid internship starting September 2027. The role is head office based requiring a minimum of 2 days a week to be worked from our office in Winnersh.

INTRODUCING THE OPPORTUNITY 

At Boehringer Ingelheim, our Patient Safety & Pharmacovigilance (PSPV) team plays a vital role in protecting patients by monitoring the safety of medicines and ensuring potential risks are identified, understood, and managed appropriately. As a PSPV intern, you will gain first-hand insight into how safety information is used to support the safe use of medicines and inform patient-centred benefit-risk decision-making. Working alongside a team of experienced PSPV professionals, you will explore how medicine safety signals and benefit-risk profiles are identified, assessed, and managed to help protect patients throughout a medicine's lifecycle. Few internships offer the opportunity to contribute to work with such a direct impact on patient wellbeing while gaining valuable insight into the science, regulation, and decision-making that underpin modern healthcare. This is an opportunity to see how patient safety, science, and medicine come together to make a real difference to patients' lives.

WHAT YOU WILL DO

Support the PSPV team in delivering key pharmacovigilance and patient safety activities that help ensure the safe and appropriate use of medicines.

Contribute to projects that strengthen patient safety processes, inspection readiness, compliance, and continuous improvement initiatives.

Collaborate with experienced patient safety, regulatory affairs, medical, quality, and compliance professionals to gain insight into how cross-functional teams protect patients.

Assist with analysing safety information, reviewing pharmacovigilance data, and preparing materials that support safety surveillance and regulatory requirements.

Learn to use pharmacovigilance systems, databases, and business tools, gaining exposure to real-world safety processes and governance frameworks.

Participate in activities that support the collection, evaluation, and communication of safety information to internal stakeholders and health authorities.

Observe and contribute to inspection readiness and quality management activities, helping maintain a culture of compliance and continuous improvement.

Develop a foundational understanding of benefit-risk management and how safety evidence informs decisions that ultimately protect patients.

Deliver a defined internship project, presenting recommendations and outcomes to the PSPV team at the end of the placement.

WHAT YOU WILL GAIN

Develop specialist knowledge of Pharmacovigilance and Patient Safety, learning how safety data is used to identify potential risks, inform benefit-risk decisions, and support the safe use of medicines.

Gain hands-on experience in a global and local healthcare environment, working alongside experienced professionals and contributing to meaningful activities that support patient safety, regulatory compliance, and continuous improvement.

Build professional skills for your future career, including data analysis and interpretation, scientific appraisal, project ownership, teamwork, stakeholder engagement, cross-functional collaboration and influencing across diverse stakeholder groups.

WHAT YOU CAN EXPECT FROM A BOEHRINGER INGELHEIM INTERNSHIP

Meaningful work and real responsibilities from the start, with opportunities to contribute to projects that matter.

Joining with a large cohort of exceptional students, you will receive a clear placement plan setting out key projects, milestones and your learning goals for the year.

Support from your manager, your team and HR, with regular feedback and development conversations.

Learning opportunities beyond the role, including workshops, networking, career insights and exposure to different parts of the business.

Access to coaching, mentoring and online learning resources, including  Boehringer’s virtual University.

The opportunity to build professional confidence, workplace skills and a network across the organisation.

ESSENTIAL REQUIREMENTS 

Currently studying for a Science, Pharmacy or Biotechnology degree and completing a placement year as part of the course.

A minimum of three A levels at grades ABB, or equivalent.

The right to work in the UK for the full duration of the internship.

The ability to travel independently to the usual place of work and, where required, to other sites.

Ability to work independently and as part of a team.

Understanding of regulatory and ethical considerations related to health data.

Strong attention to detail and commitment to data quality.

Ability to work in structured, process‑driven, regulated environments.

DESIRABLE REQUIREMENTS

Quality and Compliance Awareness.

Data handling, documentation skills, and analytical/critical thinking.

Interest in digital tools or AI‑enabled safety processes (e.g., automation, analytics).

Curiosity and understanding of Good Pharmacovigilance Practices (GVP) module and/or familiarity with local regulators such as the MHRA, HPRA, and the Maltese Authority.

Comfortable contributing to continuous improvement initiatives and/or driving or contributing to AI projects and initiatives.

SKILLS AND BEHAVIOURS

Communicates clearly and professionally in writing and conversation.

Works collaboratively, builds positive relationships and contributes own ideas proactively.

Organises tasks, manages time and meets agreed deadlines.

Takes ownership of learning, asks questions and responds positively to feedback.

Adapts to changing priorities and approaches work with curiosity and initiative.

Uses AI appropriately to deliver work. Confident with Microsoft Office and is willing to learn new systems and technology.

Acts professionally and follows relevant policies, procedures, legal obligations and health, safety and environmental requirements.

WHY THIS IS A GREAT PLACE TO WORK  

Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices. To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work

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Job details

Seniority
Intern/Fellow/Postdoc
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Bracknell Forest, United Kingdom
Employment type
Not listed

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 38 comparable Intern/Fellow/Postdoc Pharmacovigilance roles across 24 biopharma companies.

38Comparable roles tracked
38Currently active
24Companies hiring similar roles
13Countries represented

Salary context

13 of 38 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Only peer reporting · · $126,250/yr – $126,250/yr
Peer group range $126,250 – $380,650 (median $238,000)

Where these roles are based

Top locations among the 38 comparable roles

United States15
France5
United Kingdom4
Germany3
Japan3
South Korea1

+ 7 more countries

Seniority mix

9 of 38 peers have a known seniority level

Intern/Fellow/Postdoc5
Associate4

Therapeutic area mix

6 of 38 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology5
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

45%similar
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45%similar
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40%similar
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
Pharmazeut im Praktikum (m/w/d) Pharmacovigilance
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Function Therapeutic area Seniority Country
45%
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.