Explore your passions
Find Your Team
The SPRINT internships will offer a wide variety of opportunities in both emerging and established companies across the life-science industry in Connecticut. Internships available will span across scientific, commercial, finance, and administrative functions and all applicants will be eligible to participate in skill workshops.
Graduate Student Projects
This pilot program connects graduate students with paid project work at local life-science companies. Participants gain real-world experience while working up to ten paid hours per week.
Coming Soon!
Summer Internship Program
Undergraduate and Graduate
Biochemistry/Molecular Biology Intern
CMC Intern – Clinical Supplies
CMC Intern – Technical Operations
Congress & Meeting Management Intern
Copywriter Intern
Data Science Intern
Design Intern
Global Facilities & Engineering Intern
IT/AI Marketing Content Intern
Legal Compliance & Integrity Intern
Neuroscience Intern
Organ Perfusion Intern
Undergraduate Student Postings
Trevi Therapeutics| New Haven, CT (Hybrid)
Position Summary
The primary objective is to support the Finance and Accounting functions with various Finance and Accounting projects and tasks. The selected candidate should be pursuing a major in Finance or Accounting and have attentiveness to detail, good computer skills, and excellent written and oral communication skills. The goal is to help the intern develop a working knowledge of Finance and Accounting functions.
This is a paid, 24–32 hours per week internship position with a hybrid schedule consisting of 3 days in-person in New Haven, CT and one day working remotely. This position reports directly to the Controller.
Principal Responsibilities
Key responsibilities of this role include, but are not limited to:
• Participate in A/P Process including inputting of invoices, purchase orders and payments utilizing the A/P automation tool and ERP system
• Assist with the preparation of Accounting Process Documentation
• Assist in creating standardized accounting policies
• Assist in Management/BOD/SEC reporting process for quarter end
• Creation of Finance Onboarding training materials for new employees
• Provide assistance with forecasting process
Qualifications
• Intermediate computer software skills with MS Office (Word, Excel, Outlook, PowerPoint) OneDrive/SharePoint experience is a plus
• Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
• Ability to work independently and as part of a team
• Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment
Education
• High school or equivalent
• Currently enrolled full-time in an undergraduate program. Candidate must be pursuing a degree in Accounting, Finance, or a related field with coursework in progress and/or completed.
Undergraduate and Graduate Opportunities
Biochemistry/Molecular Biology Intern
Normunity| New Haven, CT
Normunity is a venture-backed biotechnology company focused on immune-oncology through the use of monoclonal antibodies to stimulate immune response in specific therapeutic targets. The Company is based on research by Lieping Chen, Professor of Cancer Research and Immunobiology at Yale University and member of National Academy of Sciences. The Company is operating at the new Biolabs facility located at 101 College Street, New Haven.
We are looking for a highly motivated and dedicated candidates for a full-time summer intern. Part-time applicants may be considered. While supervised by scientific staff, the candidate will have an opportunity to play an integral role in advancing our early therapeutic candidates into the clinic by employing immuno-oncology, cancer biology, molecular biology, and immunology techniques. The candidate will have the opportunity to experience a true start-up environment.
Key Responsibilities
- Example Responsibilities Include (but not limited to):
- Utilize public/proprietary databases (e.g., TCGA, GTEx, UniProt, etc.) and scientific literature to identify and validate novel targets associated with specific disease pathologies.
- Work with senior scientist to design and implement ELISA, biochemical and molecular biology assays.
- Organizing data, analyzing results, contributing to reports, troubleshooting assays, communicating and presenting findings
- Willingness to work in an entrepreneurial, fast-paced, hands-on environment to help establish a state-of-the-art scientific laboratory
- Troubleshooting and optimizing assays through surveying the literature, data interpretation, identification of novel or alternative procedures and techniques, and timely execution of experiments
Qualifications
- Availability to start anytime in May or June, 2026 (Full-time, In person, New Haven Connecticut)
- Ability to design, develop, and execute research activities commensurate with 3 or 4th year college science major. Graduate student research and prior internship experience is a plus
- Strong communication skills, and proven ability to collaborate in a team setting
- Ability to multi-task in a fast-paced, dynamic environment while delivering high quality work
CMC Intern – Clinical Supplies
Trevi Therapeutics| New Haven, CT (Hybrid)
Position Summary
The primary objective is to support the Chemistry, Manufacturing and Control Department in the execution of the Company’s Clinical Supply activities to ensure fully compliant delivery of clinical trial material to clinical sites. The selected candidate should be pursuing a major in a scientific field, have attentiveness to detail, good computer skills, and excellent written and oral communication skills. The goal is to help the intern develop a working knowledge of pharmaceutical manufacturing under all applicable Global Regulations and Guidances.
This is a paid, 20-40 hours per week internship position with a hybrid schedule consisting of 3 days in-person in New Haven, CT and one day working remotely. This position reports directly to the Director of Clinical Supplies.
Principal Responsibilities
Key responsibilities of this role include, but are not limited to:
• Strategies and tactics for supplying clinical sites with study drug
• Review of packaging, labelling and shipping documentation
• Support for clinical site supply and depot returns
• Monitoring of site inventory and alignment with IRT updates
• Assist with review of vendor records
Qualifications
• Basic understanding of chemical principles
• Intermediate computer software skills with MS Office (Word, Excel, Outlook, PowerPoint) and
OneDrive/SharePoint
• Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
• Ability to work independently and as part of a team
• Strong interpersonal skills including verbal and written communication are essential in this collaborative
work environment
Education
• High school or equivalent
• Currently enrolled full-time in an undergraduate or graduate program. Candidate must be pursuing a degree in Chemistry, Chemical Engineering, Biology, Pharmacy, or other related field
CMC Intern – Technical Operations
Trevi Therapeutics| New Haven, CT (Hybrid)
Position Summary
The primary objective is to support the Chemistry, Manufacturing and Control Department in the execution of the Company’s formulation development and NDA Readiness processes by assisting the Technical Operations group. The selected candidate should be pursuing a major in a scientific field, have attentiveness to detail, good computer skills, and excellent written and oral communication skills. The goal is to help the intern develop a working knowledge of pharmaceutical manufacturing under all applicable Global Regulations and Guidances.
This is a paid, 20-40 hours per week internship position with a hybrid schedule consisting of 3 days in-person in New Haven, CT and one day working remotely. This position reports directly to the Vice President of CMC.
Principal Responsibilities
Key responsibilities of this role include, but are not limited to:
• Strategies and tactics identifying new formulations
• Evaluation of manufacturing processes for compliance with current regulatory requirements
• Evaluation of analytical process for compliance with global regulations
• Review of internal company documentation for accuracy and compliance
• Preparation or review of company regulatory documents and procedures (reports, SOPs, Work Instructions, etc.)
• Assist with review of vendor records
Qualifications
• Basic understanding of chemical principles
• Intermediate computer software skills with MS Office (Word, Excel, Outlook, PowerPoint) and OneDrive/SharePoint
• Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
• Ability to work independently and as part of a team
Congress & Meeting Management Intern
Boehringer Ingelheim| Ridgefield, CT (Hybrid)
Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Congress & Meeting department located at our Ridgefield, CT campus. As an Intern, you will provide planning support across programs ranging from small-scale on campus meetings to large meetings across the US.
The Congress & Meeting Management Intern will support the planning, coordination, and execution of key internal and external events across the organization. This role offers hands‑on exposure to meeting operations, cross-functional collaboration, professional communications, and project management within a fast‑paced environment.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees
Duties & Responsibilities
-
Support meeting logistics, including personalized agendas, attendee tracking, registration oversight, and day‑of coordination.
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Maintain project tools (Planner/Teams), track tasks, update statuses, and manage team calendars and travel.
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Build or update meeting-related materials such as agendas, timelines, PowerPoint decks, and post‑meeting report packages.
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Assist with gift research, vendor comparisons, budgeting, and organizing gift distribution.
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Handle shipping preparation, including inventory, packing lists, labeling, and meeting card tracking.
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Identify process improvements and help create “how we work” guides for onboarding future hires/interns.
Requirements
- Must be a current undergraduate, graduate or advanced degree student in good academic standing.
- Student must be enrolled at an accredited college or university for the duration of the internship.
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
- Major or minor in related field of internship.
- Undergraduate students must have completed at least 12 credit hours at current college or university.
- Graduate and advanced degree students must have completed at least 9 credit hours at current college or university.
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
-
Minimum of 1 – 2 years of related experience in event planning, coordinating, and administration
• Excellent customer service orientation with ability to build and foster relationships with diverse constituencies
• Strong communication and interpersonal skills, including proficient writing and computer skills, strength in analytical and reasoning skills
• Ability to work effectively in a fast-paced, team-based, service-oriented environment
• Ability to exercise good judgment, work productively under deadlines and carry out multiple tasks with minimal supervision
• Exceptional attention to detail and the ability to perform non-routine work with changing priorities and collaborating parties, while maintaining a high level of customer service and professionalism in a fast-paced environment
• Computer literacy including proficiency in the Microsoft Office Suite
• Desire to work in a collaborative environment that values teamwork, innovation, creative problem-solving, and community engagement
Compensation:
This position offers an hourly rate typically between $20/ hour and $33/ hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Boehringer Ingelheim| Ridgefield, CT (Hybrid)
Compensation Data
This position offers an hourly rate typically between $24/ hour and $33/ hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Description
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Creative Solutions department located at our Ridgefield, CT offices. As an Intern, you will join the in‑house creative team and be paired with a Design Intern to develop HCP and consumer marketing content, assist internal projects, and potentially help shape campaign ideas.
This role is based on-site at our Ridgefield, CT location with hybrid flexibility of 2-3 days per week on-site.
Duties & Responsibilities
- Write and edit marketing copy for HCP and consumer channels e.g., brochures, e‑mails, patient materials, and social posts/banners.
- Adapt tone and messaging to meet regulatory, medical accuracy, and brand guidelines while keeping content clear and engaging.
- Support campaign concepting by developing headline and tagline options.
- Collaborate with cross‑functional partners (Creative Lead, project management, marketing, and design partner) to incorporate feedback and implement required changes.
- Assist with research and fact‑checking to ensure claims are accurate and appropriately sourced for HCP and consumer audiences.
- Contribute to ideation sessions and provide multiple creative directions under guidance from senior writers and creative leads.
- Role reports to an assigned Creative Lead on the team.
- Willing to work onsite in Ridgefild, CT at least two days a week
Requirements
- Must be a current undergraduate, graduate, or advanced degree student in good academic standing.
- Students must be enrolled at an accredited college or university for the duration of the internship.
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
- Major or minor in related field of internship.
- Undergraduate students must have completed at least 12 credit hours at their current college or university.
- Graduate and advanced degree students must have completed at least 9 credit hours at current college or university.
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
- Healthcare or life sciences familiarity: Coursework or prior writing experience in health, biology, pharma, or regulated industries.
- Marketing and campaign work: Experience drafting headlines, taglines, message frameworks, and interpreting creative briefs.
- Experience writing for digital assets.
- Tools: Familiarity with Microsoft Office; basic exposure to project management systems such as Workfront, Jira or Wrike. Be willing to adopt new platforms.
- Critical thinking: Not intimidated by scientific content to translate clinical information into audience‑appropriate language.
- Diligence: Detects inconsistencies, adheres to style guides, and produces error‑free drafts.
- Idea generation: Produces multiple creative directions and contributes constructively to ideation sessions.
- Professionalism and confidentiality: Manages sensitive information responsibly and completes required compliance training.
- Curiosity and coachability: Eager to learn medical/regulatory processes and receptive to mentoring.
Boehringer Ingelheim| Ridgefield, CT
Are you passionate about applying data science and AI to transform the discovery and development of novel biotherapeutics? Do you want to work in a collaborative and innovative environment with a global leader in human and animal health? If so, you might be the ideal candidate for the Data Science Co-op in the Biotherapeutics department at Boehringer Ingelheim.
As a Data Science Co-op, you will join the Biotherapeutics department and work on a project that leverages advanced machine learning, including protein language models to enhance the efficiency and quality of antibody engineering and biotherapeutic research. You will have the opportunity to learn from experienced scientists and engineers and contribute to the department’s AI-driven strategy for developing new biological entities (NBEs), including antibodies, proteins, and gene therapies.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees.
Duties & Responsibilities
- Collaborate with the Biotherapeutics Data Science & AI team to develop and apply generative AI and protein language models for antibody discovery.
- Design and implement deep learning and machine learning models to support predictive analytics in biotherapeutics drug discovery.
- Analyze high-dimensional biological datasets (e.g., sequence, structure, assay data) to uncover insights that inform CMC strategies and improve developability.
- Assist in building scalable pipelines for model training, evaluation, and deployment in a research setting.
- Contribute to ongoing research projects by performing literature reviews, benchmarking algorithms, and presenting findings to cross-functional teams.
- Support the development of internal tools and platforms that accelerate biologics research through automation and intelligent data integration.
Requirements
• Must be a current undergraduate, graduate or advanced degree student in good academic standing.
• Student must be enrolled at a college or university for the duration of the internship.
• Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
• Major or minor in related field of internship
• Undergraduate students must have completed at least 12 credit hours at current college or university.
• Graduate and advanced degree students must have completed at least 9 credit hours at current college or university.
Desired Experience, Skills and Abilities:
- Strong foundation in machine learning, deep learning, and statistical modeling, with coursework or project experience in bioinformatics or computational biology.
- Familiarity with protein sequence and structure data, and experience using advanced protein language models (PLMs) such as ESM-2.
- Exposure to structure prediction and generative design tools including AlphaFold, Rosetta, RFDiffusion, and ProteinMPNN.
- Experience working with antibody-specific and structural databases such as SAbDab, OAS, and PDB to support molecular modeling and developability assessments.
- Hands-on experience with graph neural networks (GNNs) for modeling biomolecular interactions and structural relationships.
- Familiarity with AI-driven approaches for modeling protein interactions, structural compatibility, and molecular design.
- Proficiency in Python and relevant libraries (e.g., PyTorch, TensorFlow, scikit-learn).
- Background or interest in antibody engineering, biologics developability, or CMC workflows is a strong plus.
- Ability to work independently and collaboratively in a multidisciplinary team environment.
Eligibility Requirements
• Must be legally authorized to work in the United States without restriction.
• Must be willing to take a drug test and post-offer physical (if required)
• Must be 18 years of age or older
Compensation Data
This position offers an hourly rate of $20 to $33 commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here
Boehringer Ingelheim| Ridgefield, CT (Hybrid)
Compensation Data
This position offers an hourly rate typically between $24/ hour and $33/ hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Description
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Creative Services department located at our Ridgefield facility. As an Intern, you will provide an opportunity for a design student to be part of a creative department learning from our team and supporting in the creation of marketing assets.
This role is based on-site at our Ridgefield, CT location with hybrid flexibility of 2-3 days per week on-site.
Duties & Responsibilities
- Design digital and print assets as assigned
- Participate in creative reviews, department meetings and weekly stand ups, speaking to assigned projects
- Manage assigned projects within project management tool, ensuring deadlines, and required approvals are met
- Participate in conceptual design projects as assigned
- Gain an understanding of BI’s requirements for MLR review
Requirements
- Must be a current undergraduate, graduate, or advanced degree student in good academic standing
- Student must be enrolled at a college or university for the duration of the internship
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred
- Major or minor in related field of internship
- Undergraduate students must have completed at least 12 credit hours at current college or university
- Graduate and Advanced Degree students must have completed at least 9 credit hours at current college or university
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
- Portfolio that demonstrates a clear graphic design point of view, understanding of design for print and digital
- Hands on experience with Adobe Suite, PPT/Google Slides a plus
- Facility with new software e.g., project management tools
- Strong communication skills, verbally and in writing
- Proactive attitude and desire to understand the design pharma landscape
Our Company
Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,500 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com
Global Facilities & Engineering Intern
Boehringer Ingelheim| Ridgefield, CT
Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Global Facilities and Engineering (GFE) Department located at our Ridgefield Campus. As an Intern, you will assist the Engineering team within GFE in directing and ensuring proper maintenance and operation of pilot manufacturing and chemical processing systems, facilities, and equipment though the design and creation of engineered system modifications. This may include preventative maintenance programs, inspections, system replacements, and budgetary requirements. In this position you will also provide technical assistance and guidance to key users and consult with outside contractors and vendors to ensure facility equipment is properly operated and maintained. You may also assist with the design and implementation of capital and maintenance projects, participate in the management and technical aspects of the projects including design, construction, and completion within budget.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees
This position offers an hourly rate of $20.00 – $33.00 USD commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Duties & Responsibilities
Work with the Boehringer Ingelheim GFE department to provide engineering and project management for a wide variety of capital projects including facility, equipment, site and utility construction, renovation projects and documentation management.
- Perform weekly check of assigned systems and revise engineering documentation as required (specifications, drawings, etc)
- Work with Engineers, Architects, Environmental Health and Safety, Designers and User Groups to support the development of project proposals, feasibility studies, design and detailed designs
- Work with external contractors and vendors to prepare quotes and estimates for on-going project work and facility modifications
- Assist with engineering design through the development of Flow Diagrams (PFDs) and Process Instrumentation Diagrams (P&IDs) per process requirements
- Under supervision of lead engineer, perform data collection and basic statistical analysis on process design conditions in support of systems optimization and troubleshooting activity
- Obtain experience developing and supporting pharmaceutical development projects, chemical process systems, site and facility utility systems, and GMP/GLP/GxP pharmaceutical regulations and practices
- Provide support to develop new systems to ensure GxP compliance and plant operator safety
- Obtain experience performing evaluations and troubleshooting existing building utilities and control systems
- Work is reviewed for adequacy and accuracy by facilities and project engineers as required
Requirements
Requirements:
- Must be a current undergraduate, graduate or advanced degree student in good academic standing
- Student must be enrolled at a college or university for the duration of the internship
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred
- Major or minor in related field of internship
- Undergraduate students must have completed at least 12 credit hours at current college or university
- Graduate and Advanced Degree students must have completed at least 9 credit hours at current college or university
Desired Experience, Skills and Abilities:
- Basic understanding of Mechanical, Electrical, Chemical, and/or Process Engineering fundamentals through coursework and projects
- Sophomore level or higher
- Strong verbal and written communication skills required
- Ability to deal professionally with internal and external customers of various organizational levels
- Ability to work effectively within a department team and members of same or higher organizational levels
- Strong attention to detail and desire to learn topics outside of typical engineering disciplines
- Demonstrated potential for technical proficiency, scientific creativity, and collaboration with others and independent thought.
- Strong computer skills with beginner level proficiency in Microsoft Word, Excel, PowerPoint
- Basic competency with AutoCAD
- Ability to work effectively with minimal supervision
- Hands-on experience with mechanical/electrical/plumbing/chemical, management systems
- Knowledge of GxP regulations and chemical processing
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required)
- Must be 18 years of age or older
Legal Compliance & Integrity Intern
Boehringer Ingelheim| Ridgefield, CT (Hybrid)
Compensation Data
This position offers an hourly rate of $24-33/hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Description
Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Legal & Compliance department located at our Ridgefield, Connecticut facility. As an Intern, you will learn about Compliance and Legal in the Pharmaceutical Industry and the effective elements of a Compliance Program by assisting the Compliance & Integrity and Legal team on dynamic projects overseen by experienced compliance and legal professionals. As an intern, you will gain cross functional exposure through collaboration with various departments at Boehringer Ingelheim. This will include the opportunity to meet and interact with experienced professionals with varying backgrounds and expertise, as well as gain exposure to Boehringer Ingelheim’s products, businesses, and culture.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees
Duties & Responsibilities
- Complete and support various assignments/projects/initiatives across the Compliance & Integrity and Legal function, including the preparation of documents, reports, and presentations, as applicable
- Attend/participate in meetings when included by the Compliance & Integrity and Legal team
- Collaborate with various members of Boehringer cross-functionally to support initiatives
- This is a hybrid role for the department supporting both compliance and legal
Requirements
- Must be a current undergraduate student in good academic standing
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
- Major or minor in related field of internship/co-op.
- Undergraduate students must have completed at least 12 credit hours at current college or university.
- Graduate and advanced degree students must have completed at least 9 credit hours at current college or university.
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
- Interest in pharmaceutical and/or healthcare industry, as well as Legal and/or Compliance focus
- Ability to collaborate across the organization, working both as part of a team and as an individual
- Able to work independently and deliver results with minimal supervision
- Detail oriented, self-starter, accountable and agile
- Strong communication skills, both oral and written
- Skilled project planning and organizational mindset
- Some level of work experience demonstrating good judgment
Our Company
Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,500 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com
IT/AI Marketing Content Intern
Boehringer Ingelheim| Ridgefield, CT
Compensation Data
This position offers an hourly rate of $24-33/hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Description
Boehringer Ingelheim is currently seeking talented and innovative internship candidates to join our IT M&S Omnichannel department, working at our corporate U.S. headquarters in Ridgefield, CT. As a member of the IT M&S team, you will be responsible for researching technologies and evaluating opportunities to deliver value to the IT M&S Omnichannel portfolio of systems and services through the development of AI-enabled applications that enhance business value and drive commercial success. Internship candidates will work with a global team of colleagues to deliver innovative solutions in the areas of AI, Data Science, Software Engineering, APIs, IoT, business intelligence and/or other state-of-the-art technologies in support of our company’s operations and decision-making processes.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence allows all employees to collaborate internationally, offering visibility and the opportunity to directly contribute to the company’s success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
This role will be on-site 3 – 5 days per week in our Ridgefield, CT location, and interact with a globally-diverse team of colleagues and support staff. This position is for Summer 2026.
Duties & Responsibilities
- Collaborate with business partners to collect application user requirements, as well as ideas for application/process improvements.
- Propose IT-centered enhancements, technology use-cases, and/or solutions.
- Execute the PoC/pilot projects using Agile methodologies and framework.
- Upon execution of the pilot project(s), document the solution design, and transfer the necessary knowledge and lessons learned to IT support team.
- Support business partners with technology-related needs.
Requirements
- Must be a current undergraduate, graduate or advanced degree student in good academic standing.
- Student must be enrolled at an accredited college or university for the duration of the internship/co-op.
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
- Major or minor in related field of internship/co-op.
- Undergraduate students must have completed at least 12 credit hours at current college or university.
- Graduate and advanced degree students must have completed at least 9 credit hours at current college or university.
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
- Experience with programming languages such as Python and frameworks (e.g., Streamlit), as well as using and writing APIs.
- Experience with using LLMs programmatically.
- Experience with Marketing and Sales applications (e.g., MRL) or processes.
- Experience implementing Data Science projects preferred (e.g., training ML models, fine-tuning models, (un)supervised learning.
- Experience with development tools such as IDEs, Jira, Confluence, and Bitbucket (Git) preferred.
- Experience with cloud-based systems preferred.
- Self-driven, independent and curious with good communication skills.
- Ability to relate technology-related information to non-technical audience.
- Ability to prioritize, and work with colleagues around the world.
Arvinas| New Haven, CT
We are looking for a motivated individual to work as a summer intern (May 19 to August 15) within Neuroscience. This position will be focused on development of cellular and biochemical assays to support one of our preclinical programs. Under the guidance of staff, the intern will implement basic scientific techniques at the bench, critically read, process, and present selected papers from the relevant scientific literature, and a summary of their work at an end-of-summer student colloquium. This position reports to a Research Investigator or another member of the Neuroscience group.
This will be a full-time, on-site position located at our headquarters in New Haven, CT.
Principal Responsibilities
Key responsibilities of this role include, but are not limited to:
- >75% lab work: conduct experiments and analytical assays involving cell culture, protein detection, or protein:ligand interactions.
- Execution of assays to query targeted protein degradation: western blots, ELISA, reporter assays, etc.
- Use of lab automation for compound handling.
- Learn protein degrader pharmacology and data analysis.
- Apply excellent organizational skills to maintain lab stocks and lab cleanliness.
- Maintain clear experimental records and communicate well with supervisor and other team members.
- Deliver critical data by following provided protocols and guidance.
Qualifications
- Motivated and productive individual with excellent communication skills who works effectively in a team setting.
- Prior lab experience is required.
- Experience with aseptic mammalian cell/tissue culture is required.
- Experience with antibody-based detection of proteins is strongly preferred.
- Some experience with 96- or 384-well plate-based assays is preferred (e.g., ELISA, colorometric assays, cell growth assays).
- Basic understanding of cell biology, molecular biology, and biochemistry through coursework.
- Organized, goal-oriented, and timeline-conscious.
- Other preferred skills and knowledge.
- Experimental documentation/lab notebook.
- Data presentation.
- Experience with Microsoft Office suite (Word, Excel, PowerPoint).
- A strong work ethic and willingness for continued learning.
- Arvinas will not be providing VISA sponsorship for this position. You must have the ability to work without the need for a current or future VISA sponsorship.
- The duties of this role are generally conducted in a lab environment. Employees must be able, with or without an accommodation to lift/carry 15/30 pounds unassisted/assisted; work comfortable in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.
Education
- Current 3rd or 4th year undergraduate or graduate student with a background in biological sciences and an interest in Neuroscience.
Revalia Bio| New Haven, CT
Revalia Bio is seeking to revolutionize biomedical innovation by creating the world’s first integrated human data stack
Revalia Bio is a forward-thinking digital health, tech startup building the world’s first integrated human data stack to modernize biomedical innovation by enabling a new class of digitally enabled Phase 0 Human Trials.
Revalia’s Phase 0 Human Trial platform integrates various sources of human data to ask and answer questions that are impossible with current Phase I/II clinical trials or preclinical models alone. The key to the platform is Revalia’s ‘Human Organ Data Layer’ made possible by a unique network of partnerships assembled to support organ donation for research when those organs are not suitable for clinical transplant. The Revalia team brings those organs back to life on proprietary organ perfusion technology to create a ‘Rosetta Stone’ for human data that serves to integrate and contextualize all other sources of human data from patient medical records to cells in a petri dish.
Revalia provides access to the Phase 0 Human Trial through a Platform as a Service model that enables biomedical developers to design, track and interpret Phase 0 Human Trials at the click of a button guided by Rio, Revalia’s software companion. Through this new platform, Revalia aims to enable the global biomedical community—from academic scientists and hospitals to large biopharma—to effectively collaborate on creating better medicines faster. The team at Revalia believe that biomedical innovators should compete on delivering the best innovations to patients as fast as possible, not on access to critical human data.
Revalia Bio is seeking a skilled and driven Organ Perfusion Intern with a strong background in clinical or clinical-adjacent settings. This role involves supporting advanced organ perfusion studies using donated human research organs. Specialists are responsible for preparing organs for perfusion, assisting in surgical benching, and operating sophisticated perfusion and point-of-care diagnostic equipment.
We are specifically looking for experienced healthcare professionals- including nurses, paramedics, surgical techs, laboratory technologists, and others with a clinical mindset, who are excited to contribute to cutting-edge biomedical innovation in a research setting
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Key Responsibilities
- Train to perform ex vivo perfusions of human lungs, livers, and kidneys
- Assist with surgical benching and dissection to deepen understanding of human anatomy
- Operate clinical-grade perfusion circuits and monitoring systems
- Collect, process, and log biological samples (e.g. blood, biopsies, urine, bile)
- Participate in translational research by evaluating new therapeutics in human models
- Maintain equipment and manage laboratory supply inventory
- Document procedures and results with precision in both paper and digital formats
- Ensure a clean, safe, and compliant lab environment
- Participate in a rotating on-call schedule.
Preferred Background
- Clinical experience (e.g. RN, OR Tech, Surgical PA, Medical Assistant or similar healthcare roles)
- Familiarity with laboratory protocols, POC testing, and handling biohazardous materials
- Strong understanding of sterile technique and safety standards
- Able to work in a dynamic, high-pressure environment independently and on a team
- Comfortable with technology, including MS Office and database entry
- Undergraduate degree in biology, nursing, biomedical science, or a related field
- Excellent physical stamina and attention to detail
Who You Are
- You’re a medical professional looking to apply your clinical training in a pioneering research setting
- You’re curious, collaborative, and eager to learn surgical techniques and perfusion science
- You thrive in fast-paced environments and are committed to advancing medical innovation
- You embrace feedback and view it as a path toward professional growth
Compensation and Hours
This position will pay an hourly rate of $20/hr for 20 hours maximum of work per week. This internship will extend 10 weeks throughout the summer.
Graduate Student Postings
Boehringer Ingelheim| Ridgefield, CT (Hybrid)
Compensation Data
This position offers an hourly rate of $24-33/hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Description
Boehringer Ingelheim is currently seeking a talented and innovative Summer Law School Intern to join our Legal Department located at our Ridgefield, CT facility. As a Summer Intern, you will support the Legal Department and related business functions including promotional review, contract review, litigation and risk assessment, and intellectual property assessments. You will learn critical skills to advise business operations in pharmaceuticals and work in a highly regulated industry.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the company’s success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
Duties & Responsibilities
Assignments and projects will be overseen by experienced legal professionals and staff. As an intern, you will gain cross functional exposure through collaboration with various departments at Boehringer. This will include the opportunity to meet and interact with seasoned professionals with varying backgrounds and expertise as well as gain exposure to Boehringer Ingelheim’s products, businesses, and culture. Intern responsibilities will include the following:
- Research
- Developing presentations and PowerPoint slide decks
- Attending meetings
- Interacting with business partners across the organization
- Interacting with outside legal counsel
Requirements
- Must be a law student in good academic standing.
- Must have completed 12 credit hours from an accredited law school (or have completed 1 or 2 years of law school).
- Overall cumulative GPA from last completed quarter 3.0 GPA (on a 4.0 scale) preferred.
- Student must be enrolled at an accredited college or university for the duration of the internship/co-op.
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
- Major or minor in related field of internship/co-op.
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
- Must possess strong verbal, written, presentation and other communication skills.
- Must demonstrate ability to collaborate and partner across the Legal Department (including the Human Pharma Business Law, Intellectual Property, Legal Operations and Employment and Litigation groups).
Platform Biology Summer Intern
Arvinas| New Haven, CT
The Platform Biology summer internship position at Arvinas will focus on evaluating and developing 3D biology to include automation and high-content imaging to support Oncology and Neuroscience. This position will involve cell biology and biochemical techniques, use of automation equipment, and high-content imaging. The candidate will join a collaborative, multi-disciplinary team of biologists, biochemists, biophysicists, and chemists. This is a laboratory-based role that will work to automate the biology and staining of 3D spheroids (and possibly organoids) for deeper understanding of and screening for novel PROTACs. We are looking for a passionate and highly motivated individual who is enthusiastic about novel therapeutic applications, such as degraders, and wants to contribute to exploring new modalities of targeting proteins for degradation across neuroscience, oncology and immune-oncology space.
This training opportunity allows the individual to learn the process of early drug discovery in a collaborative environment.
This position reports to a Senior Research Scientist, Platform Biology and will be located at our headquarters in New Haven, CT.
Principal Responsibilities
Key responsibilities of this role include, but are not limited to:
- Cell culture including sterile technique for mammalian cell lines
- Live-cell assays to monitor, image and analyze 3D spheroids
- Cellular assays working to fix, permeabilize, and use immunofluorescence staining to research methods for 3D spheroid marker infiltration including tissue clearing while automating the staining process
- Develop, run and analyze data using high-content imaging instruments
- Cellular assays to monitor activity of degrader compounds (such as JESS, high-content, luminescence, fluorescence, NanoBRET)
- Data analysis and interpretation, as well as presenting data in team meetings.
- Meeting with key stakeholders outside of the project team to devise future experiments for downstream applications
- Major areas of focus will include utilizing established workflows to guide assay development and technical optimization, evaluating appropriate controls, and troubleshooting.
Qualifications
- The candidate should be a highly motivated fast learner with flexibility and ability to multi-task, as well as a good lab citizen.
- Previous oncology or neuroscience experience is preferred
- Experience in cell culture is required.
- Experience with microscopy and high content imaging is a plus.
- Knowledge of ubiquitin-based proteasomal degradation is desired, but not a pre-requisite.
- Ability to work full-time (40 hours per week).
- Arvinas will not be providing VISA sponsorship for this position. You must have the ability to work without a need for a current or future VISA sponsorship.
- The duties of this role are generally conducted in a lab environment. Employees must be able, with or without an accommodation to lift/carry 15/30 pounds unassisted/assisted; work comfortable in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.
Education
- Preference to Master’s / PhD student currently enrolled in a program with a concentration in cell biology, immunology, pharmacology, biology, or related fields.
- Prior laboratory experience is a plus.
Preclinical Formulations Intern
Boehringer Ingelheim| Ridgefield, CT
Compensation Data
This position offers an hourly rate of $24.00 – $33.00 USD / hour commensurate to the level of degree program in which an applicant is actively enrolled. For an overview of our benefits please click here.
Description
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Preclinical Formulations, Non-clinical Safety Sciences department located at our Ridgefield, CT facility. As an Intern, you will learn about the strategies used in early-stage formulation development and influence of formulation type on the outcome of a non-clinical study. Development and delivery of robust preclinical formulations encompasses unique challenges. The internship will provide an opportunity to learn about the approaches to address these challenges in an industrial setting.
Duties & Responsibilities
• Review formulation strategies for non-clinical studies.
• Provide support for formulation preparation for early-stage non-clinical studies.
• Perform database and/or literature search as necessary.
Requirements
- Must be a current graduate or advanced degree student in good academic standing.
- Student must be enrolled at an accredited college or university for the duration of the internship.
- Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred.
- Major or minor in related field of internship.
- Graduate and advanced degree students must have completed at least 9 credit hours at current college or university.
Eligibility Requirements:
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
Desired Skills, Experience and Abilities
• Ph.D. or Master’s student in Pharmaceutical Sciences or equivalent
• Familiarity with general principles of preformulation and formulation development
• Ability to work in laboratory independently.
• Ability to think critically about experimental results and draw conclusions
• Effective written, communication and interpersonal skills
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