Agios Pharmaceuticals Internships - 164 jobs

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 Health Economics and Outcomes Research (HEOR) Value Demonstration. As an Intern, you will be deeply involved with the HEOR team, working with colleagues with understanding and shaping the value proposition of our cardiovascular, renal, and metabolic assets and pipelines. The intern will work cross-functionally, collaborating with medical, value and access, epidemiology, and real-world evidence teams to design and implement health economic models and outcomes research studies. Through direct experience and mentorship, the intern will gain profound insights into the essential role of HEOR in formulating a market access strategies. The internship will be remote. **Duties & Responsibilities** + **Support Diverse HEOR Study Types:** Assist in conducting a variety of HEOR study types, including retrospective claims analysis, electronic medical record database evaluations, cost-effectiveness and budget impact modeling, meta-analysis, and systematic literature reviews. + **Contribute to Research Processes:** Play an integral role in all aspects of research, from conceptualization and protocol development to statistical analysis, supplier management, and dissemination of findings. + **Strategic Planning:** Work closely with HEOR colleagues and cross-functional business partners to understand and develop strategic and tactical plans that align with the business objectives of each respective therapeutic area. + **Assist with Material Creation:** Collaborate with internal HEOR colleagues to create impactful slide decks and other materials tailored for both internal and external audiences. + **Engage in Team Meetings:** Actively participate in team, department, and cross-functional meetings to deepen your understanding of the role of HEOR within the pharmaceutical industry and at Boehringer Ingelheim. **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** + _Prior research experience with conducting literature reviews, economic modelling, and real-world evidence studies._ + _Relevant advanced coursework in areas such as, but not limited to, health economics, epidemiology, biostatistics, and/or research methods._ + _Demonstrated excellent oral and written communication skills._ + _Demonstrated track record of leading teams with multiple stakeholders._ All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The Computational Oncology team drives innovation by transforming ‘omics and biomarker data into actionable insights that accelerate Takeda's Oncology pipeline. As part of the Precision and Translational Medicine organization, we collaborate across disciplines to decode complex datasets and shape strategies for personalized cancer therapies. Our mission is to improve patient outcomes by integrating cutting-edge analytics with translational science in a dynamic, purpose-driven environment. In this role, the candidate will collaborate with cross-functional teams to design and execute independent analyses using proprietary tumor datasets. They will integrate gene expression, protein abundance, and genetic mutation data to support precision medicine strategies. This hands-on experience offers the opportunity to contribute to personalized cancer treatment and make a meaningful impact on patient outcomes in a highly collaborative and innovative setting. How You Will Contribute: Collaborate with scientists across oncology, bioinformatics, and translational medicine, contributing to cross-functional research initiatives and gaining exposure to diverse perspectives in cancer research. Develop and apply innovative methods for integrating and analyzing multi-omics tumor data, using approaches such as statistical modeling and machine learning to uncover novel insights. Combine proprietary datasets with known biological pathways, networks, and interactions to explore mechanisms of treatment response and resistance. Identify molecular subtypes of cancers to support precision medicine strategies, including patient stratification and biomarker discovery. Design and execute your own integrative multi-omics analysis, tailored to your interests and experience, with guidance from experienced mentors. Internship Development Opportunities: Gain hands-on experience applying bioinformatics skills to high-quality proprietary datasets, contributing to real-world oncology research. Learn about the Oncology drug development process and discover how computational biology informs key decisions in precision medicine. Engage with leading industry professionals, gaining insights into the impact of your work and exploring career paths in translational science and the pharmaceutical industry. Job Requirements: This position will be Hybrid (1-3 days/week in office) out of the Cambridge, MA location Must be pursuing a Doctoral Degree in Computational Biology, Bioinformatics, Computer Science, or a related field Strong foundation in biology, chemistry, biochemistry, biostatistics, or a related scientific field Hands-on experience or coursework in bioinformatics, with exposure to transcriptomics, proteomics, or genetic mutation analysis Proficiency in R Interest in applying 'omics data to real-world healthcare and drug development challenges Clear and effective communication skills, with the ability to work well in cross-functional teams Strong analytical thinking and problem-solving abilities Ability to write clean, reproducible code and document analyses for collaborative research Internship Eligibility Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship Must be currently enrolled in a degree program graduating December 2026 or later The internship program is 10-12 weeks depending on the two start dates (May 26th-August 14th or June 15th- August 21st) The intern must be able to commit to one of thesetime frames Able to work full time 40 hoursa week during internship dates Takeda does not provide a housing stipend or relocation support for the U.S Summer Internship Program Program Highlights: Hands-on experience with real projects and responsibilities Dedicated mentorship program pairing interns with experienced professionals Networking opportunities with industry professionals and fellow interns Internship events focused on professional and skills development Exposure to multiple business areas or departments within a Pharmaceutical Organization Takeda Compensation and Benefits Summary We understand compensation may be an important factor as you consider an internship opportunity. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: Boston, MA U.S. Hourly Wage Range: $21.00 - $46.00 The estimated hourly range reflects an anticipated range for this position. The actual hourly wage offered will depend on the candidate's school year/level to be entered following completion of internship. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. internship benefits vary by location and may include: Paid sick time Civic Duty paid time off Participation at company volunteer events Participation at company sponsored special events Access to on-site fitness center (where available) Commuter Benefit: To offset your work-commute expenses, Takeda provides U.S. employees with a fixed monthly subsidy to be used for either public transportation (transit) or parking. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypePaid Intern (Fixed Term) (Trainee) Time TypeFull time Job Exempt NoIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Role Overview & Key Functions: This role will support continuous product supply for Karyopharm' s drug products (IMP) utilized in clinical trials. The individual will work with teams managing internal and external tasks and customers in order to accomplish project objectives and to understand the needs of the clinical trials. The Clinical Supply Chain Intern will support Clinical Supply Chain initiatives and continuous improvement activities. Responsibilities * Participate in cross-functional Project Team Meetings * Partner with PM to review, understand the Clinical Supply study process * Shadow the PM who coordinate and monitor label development process and packaging timelines with the vendors * Partner with the IRT Team to understand Randomization for Clinical Trial Studies * Manage temperature excursion process * Generate Quarterly Reports and the KPTI Performance and Risk Indicators * Overview of Commercial Global Supply Chain process * Organize and file various trial related documents Qualifications * Currently enrolled college (bachelor's program) student * Must be highly organized and have the ability to work in independently and collaboratively as a team * Must be able to complete the Karyopharm Internship Program 28May - 09Aug2024 Required Skills * Clear, concise verbal & written communication * Curious and willing to learn and use new tools / skills. * Proficiency in Microsoft Word, Excel, PowerPoint * Familiarity with advanced Excel tools * Familiarity with Process mapping * Zoom & Microsoft teams. Candidate Profile & Requirements: * Must be able to complete the Karyopharm Internship Program 27 May - 08 Aug 2025 * Currently enrolled high school or college (bachelor's program) student * Student must be returning to school in the Fall Term. * Must have a minimum GPA of 3.0 * Must be highly organized and have the ability to work in independently and collaboratively as a team * Clear, concise verbal & written communication Pay for internships ranges from $22 to $30 per hour, depending on the student's academic level (e.g., Bachelor's, Master's) and year in school. Our Value Proposition: At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!

Kickstart Your Career at Vertex! Are you ready to make a real impact? At Vertex, our mission is to tackle serious diseases and to change lives, for the better, for the future. Our aim is to give you the skills, insights, and career guidance to be an important part of that future; to turn your potential into progression. As a Vertex intern or co-op, you'll work on meaningful projects, collaborate with talented teams, and learn from industry leaders. We're passionate about innovation, inclusion, and supporting your growth-inside and outside the lab. Why Vertex? * Real Projects: You'll work on assignments that make a real impact, not just busy work. * Mentorship & Networking: Connect with leaders and peers who want to see you succeed through professional networks, connections, and collaborations that will shape your longer-term career. * Flexible & Supportive: We offer flexible work options with Flex @ Vertex and prioritize your wellbeing. * Inclusive Culture: Collaboration and inclusion are embedded in everything we do. * Career Launchpad: Build skills, explore career paths, and get guidance for your future career. Ready to apply? Submit your application and let's turn possibilities into reality! Your Impact The Vertex Statistical Programming internship program is a multi-week experiential training program for students currently working towards an advanced degree in Computer Science, Statistics, Biostatistics, Data Science, or a related field of study. If you are passionate, collaborative, and growth-minded, an internship at Vertex will help you gain meaningful experience in our biostatistics functional areas and serve as a launchpad for your career. Important Notice Regarding Internship and Co-op Inquiries At Vertex Pharmaceuticals, we are committed to providing a fair and structured recruitment process for all students interested in internship and co-op opportunities. To ensure consistency and equity, all student applications must go through our Early Talent Acquisition Team. Due to the high volume of interest, we are unable to respond to individual solicitation. Direct solicitation to Vertex employees- including senior leaders via email will result in removal from the recruiting process. We appreciate your enthusiasm and interest in Vertex. To be considered for internship or co-op roles, please apply directly through our official application channels. (************************************************************************** Thank you for respecting our process and helping us maintain a fair experience for all candidates. What you will be doing: In this 12-week summer Internship program, the SP intern will work closely with Statistical Programmers and biostatisticians, especially Biometrics AI_working_group for AI and ML in Clinical Trials, such as interactive and automated CSR QC Agent, the biometrics E2E_R_automator APP, etc. The SP intern will also have opportunities to be exposed to the drug development process and daily work of Statistical Programmers or biostatisticians in a fast-paced biotechnology company. Key responsibilities include: * Retrieval-Augmented Generation (RAG) / Tool Calling / Function Calling * Prompt Engineering / Semantic Search / Context Retrieval * LLM Agent / AI Agent / LLM APIs (OpenAI, Azure OpenAI) * Chatbot Development (internal tools) / Embedding Models * R Shiny This role requires applied LLM systems tied to R-based analytics tools (Shiny app). Focus on models, not usage. * Basic software engineering skills will be a plus, such as the ability to implement key UI features including: File upload/download (Excel, Word, RTF); Dropdown menus, text input fields, editable tables; Dynamic code editor panel (e.g., via {shiny Ace}); Workflow navigation (tabs or step-by-step). * (Complementary skills) Knowledge of Clinical Data Flow or Pharma Context, knowledge of data science, SAS, R, or Python, · (Complementary skills) NLP, Semantic Search, Embeddings, APIs, Git/GitHub * Enjoy exploring programming details and learning know technologies * Present research results and learnings to the Statistical Programming department and broader audience at departmental seminars and/or company poster sessions. * Summarize the work for future departmental use and potentially produce a peer-reviewed publication. * Attend seminars and other company activities to enhance the understanding of the drug development process and daily work of either statistical programmers or biostatisticians in a biotechnology company. What you will need to succeed: * Currently enrolled in a graduate-level curriculum leading to a Ph.D. in Computer Science, Statistics or Biostatistics or other quantitative science (e.g., data science, etc.) * Currently enrolled in a Master degree in Computer science, Statistics or Biostatistics or other quantitative science (e.g., data science, etc.) * Be in good academic standing within your graduate program and at your university. * Legal authorization to work in the United States, now and in the future. Please note that Vertex does not provide sponsorship for internships or entry level roles within this part of the organization. * You must be available to work full-time, 40 hours per week from May - August 2026 * Preferred Qualifications: * Possess a tracked record of accomplishment, including publications, awards, presentations, coding projects. * Experience with natural language processing and python is preferred but not required. * Have excellent communication, presentation, and leadership skills. * Have actual project experience in software development. * Demonstrated experience with cross-disciplinary application of statistical methods. * Genuine interest in clinical development and regulatory affairs. Program Details: * Full-time, paid internship $26.00 - 50.00 USD/hour * Program Dates: May - August 2026 At Vertex, we believe that when you feel your best, you can perform at your best. That's why our US benefits and global well-being resources are designed to support you. * Free 24/7 onsite gym access and free access to group exercise classes * Subsidized commuter benefits- transit and parking * Provided meals-free breakfast daily! * Career development opportunities and events, including C Suite engagement * Social events-both intern-only and company-wide * Location-specific perks and extras! * Recognition of National Intern Day Equal Opportunities Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Vertex is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Accessibility & Accommodations We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Vertex is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com. Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role, Vertex is unable to sponsor non-U.S. persons to apply for an export control license. This job posting is for a temporary role with a third-party agency partner that provides services to Vertex. The individual selected for this role will be offered the role as an employee of that third-party agency; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency upon offer. For any questions or concerns, please contact early_*************** Pay Range: $0 - $0 Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more. Flex Designation: Hybrid-Eligible Or On-Site Eligible Flex Eligibility Status: In this Hybrid-Eligible role, you can choose to be designated as: 1. Hybrid: work remotely up to two days per week; or select 2. On-Site: work five days per week on-site with ad hoc flexibility. Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time. #LI-Hybrid Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

Role Overview & Key Functions: As a Karyopharm, reporting to the Executive Director, GMP (Good Manufacturing Practice) Quality, you will positively impact patients' lives by: Assisting with Quality Unit (QU) efforts and activities within the organization and the Contract Service Providers, including the development and implementation of the programs. You will provide help to GMP Quality and Quality Management Systems teams, in support of the Annual GMP Quality Management Review (QMR), training program improvements, Veeva Vault processes and other ancillary quality activities. Responsibilities Participate in following activities to support GMP Quality Operations: * Assist GMP in data collection and report generation for Annual Quality Management Review (QMR). This project will require creation of excel lists, statistical analysis, and technical writing. This will give an individual overview of drug manufacturing and testing processes along with affiliated regulations and guidelines. * Assist in management of minor product quality investigations in Veeva Vault. This project will require individuals to learn and execute documentation for quality event investigations. * Develop Smartsheets and trackers for GMP Quality to better manage project deliverables and timelines. * Assist GMP Quality group in continuous improvement projects by participating in SOP revisions and process optimization. * Maintain deviation and change control lists and assist in notification of change controls to Karyopharm's global partners. * Provide communication support for training notifications and scheduling training for Karyopharm's business partners. * Assist Quality Management Systems team with revision of the training management program including updating training matrices, creating excel of GxP processes; training requirements and required training per functional team in support of Veeva configuration updates. * Support review of batch documentation and analytical data review received from CDMOs (Contract Drug Manufacturing Organizations) for various manufacturing and testing operations of Karyopharm's product. Qualifications * Enrolled into undergraduate or graduate programs in scientific disciplines with interest to learn highly regulated drug manufacturing process, analytical testing, and quality oversight. * Previous experience in Pharmaceutical or Biotech organizations is desired but not required * Good Oral and Written communication skills. * Highly proficient with MS Office tools. * Ability to learn and adapt with ambiguity of strengths. * Work in a team setting adopting collaborative and learning approach for achieving results. * Enthusiasm to learn new skills and Motivation towards career development. Candidate Profile & Requirements: * Must be able to complete the Karyopharm Internship Program 27 May - 08 Aug 2025 * Currently enrolled high school or college (bachelor's program) student * Student must be returning to school in the Fall Term. * Must have a minimum GPA of 3.0 * Must be highly organized and have the ability to work in independently and collaboratively as a team * Clear, concise verbal & written communication Pay for internships ranges from $22 to $30 per hour, depending on the student's academic level (e.g., Bachelor's, Master's) and year in school. Our Value Proposition: At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!

Role Overview & Key Functions: This internship offers a high-impact opportunity to work across multiple functions at Karyopharm, with exposure to Strategy & Portfolio Management, Business Operations, and Program Management. The intern will play a key role in evaluating and enhancing Program Team resources that define the drug development end-to-end process, ensuring they are accurate, up to date, and easily accessible. A major focus will be assessing usage patterns and upgrading the Program Team intranet site-improving content quality, presentation, navigation, and overall user experience. The intern will collaborate closely with Program Team members and functional stakeholders to gather feedback, synthesize insights, and translate them into a structured update/upgrade plan. Key deliverables include refining Karyopharm's drug development process materials, developing and executing an awareness and engagement campaign for the intranet site, and building practical skills in stakeholder feedback collection, analysis, and implementation. This role provides hands-on experience in cross-functional collaboration, strategic communication, and operational excellence within a dynamic biotech environment. Responsibilities: * Understand the interplay between different departments in drug development and commercialization (e.g. Clinical Operations, Medical, Pre-clinical, MSLs, Regulatory, Research, Drug supply, Market Access, Commercial, HEOR, Medical Affairs, Publications, Corporate Communications, Investor Relations, Launch Excellence, Patient Advocacy, Alliance Partners as well as Investigators, and Patient Advocacy groups). * Assess current drug development end-to-end process materials for accuracy and currency * Assess current usage patterns/upgrade an intranet site that serves as a central hub, providing essential resources and tools to empower Program Teams as they navigate each stage of the development process. * Gather and synthesize feedback on content and user experience from Program Team members * Establish and drive a Program Team TEAMs Site/SharePoint Engagement Campaign to further increase awareness, tool adoption, and collaboration * Create bite-sized content on high performing team best practices that elevate our values (e.g. best practices around meetings, collaboration, alignment, decision making and recognizing Program Team and/or Functional achievements) which can be included on the intranet site and in Karyopharm internal communications outlets. * Support cross-functional integrated program planning via creating and updating timeline templates, as well as templates for translating timelines into various reports and visual materials * Other Program Management Office related deliverables as prioritized by the business at that time. Qualifications: * Currently pursuing a Master's. * Ability to collaborate and interact with individuals at all levels. * Performs well under pressure and delivers results. * Communication Skills: Website development, powerpoint presentation design, content creation * Awareness of core pharmaceutical business metrics; good knowledge of current affairs. * Strategic, critical and creative thinking skills; Sound judgment and impeccable discretion in handling sensitive and confidential information. Candidate Profile & Requirements: * Must be able to complete the Karyopharm Internship Program 27 May - 08 Aug 2025 * Currently enrolled high school or college (bachelor's program) student * Student must be returning to school in the Fall Term. * Must have a minimum GPA of 3.0 * Must be highly organized and have the ability to work in independently and collaboratively as a team * Clear, concise verbal & written communication Pay for internships ranges from $22 to $30 per hour, depending on the student's academic level (e.g., Bachelor's, Master's) and year in school. Our Value Proposition: At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* **Job Function:** Career Programs **Job Sub** **Function:** Non-LDP Intern/Co-Op **Job Category:** Career Program **All Job Posting Locations:** Cambridge, Massachusetts, United States of America, La Jolla, California, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America **Job Description:** Johnson & Johnson Innovative Medicine is recruiting for multiple Clinical Pharmacology and Pharmacometrics summer interns at its US (Spring House PA, Raritan NJ, Titusville NJ, Cambridge MA and La Jolla CA) sites. Clinical Pharmacology and Pharmacometrics (CPP) is an integrated part of the Global Development organization within Johnson & Johnson Innovative Medicine. Members of CPP work in cross-disciplinary compound development teams and apply Clinical Pharmacology principles and pharmacometrics methodologies across the R&D portfolio to enable optimal decision-making in drug development. The CPP Summer Internship Program provides a unique opportunity for students passionate about drug development to collaborate with clinical pharmacologists and pharmacometricians and gain hands-on experience in CPP principles, including pharmacokinetics/pharmacodynamics (PK/PD), translational modeling, and model-informed drug development (MIDD) within a dynamic pharmaceutical R&D environment. Our teams leverage students' academic backgrounds while fostering their professional development, providing firsthand experience in drug development and an opportunity to evaluate the student's potential for future employment. CPP summer interns will contribute to diverse Research and Development efforts spanning preclinical to early- and late-stage clinical development, through activities such as: + Clinical Pharmacology and Medical literature review + Data analysis of PK, biomarker, preclinical and/or clinical data, trial design, etc. + PK and PD model-building and analyses + Development of computer programs or state-of-the-art quantitative methodologies (e.g., population PK/PD, quantitative systems pharmacology [QSP]) + Model based meta-analysis (MBMA), advanced data visualization (e.g., RShiny), and machine learning applications integrating publicly reported and in-house data + Therapeutic areas of immunology, oncology, neuroscience, cardiopulmonary and metabolic diseases **Qualifications** + Candidates must be enrolled in an accredited college or university (not necessarily taking classes) pursuing a **MS, PharmD, PhD, MD** or similar degree in a life sciences-related discipline such as Pharmacology, Pharmacometrics, Pharmaceutical Sciences, Molecular or Computational biology, Biophysics, Biostatistics, Mathematics, Engineering, or Medicine. + Candidates should demonstrate computational proficiency, including experience with data analysis, modeling, and simulation tools such as NONMEM, Phoenix WinNonlin, Monolix, R, Python, or MATLAB. + Candidates must be available to work full-time for at least 12 weeks between May - September 2026. + Candidates must be detail-oriented, highly organized, and capable of managing multiple tasks efficiently. + Candidates must have strong communication and presentation skills. + Candidates must have the ability to work independently as well as collaboratively within a team. + Candidates must be eligible to work in the US for the entirety of their internship period and will be required to provide proof of work authorization. Remote work flexibility may be available. Housing stipend will be available. Permanently authorized to work in the U.S., must 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 requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. _Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation,_ _external applicants please contact us via_ _*******************/contact-us/careers_ _. internal employees contact AskGS to be directed to your accommodation resource._ **Required Skills:** **Preferred Skills:** **The anticipated base pay range for this position is :** $23.00/hr to $51.50/hr Additional Description for Pay Transparency: The expected pay range for this position is between $23.00 per hour and $51.50 per hour but will be based on candidate's program year, discipline, degree and/or experience. Co-Ops/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan. Co-Ops and Interns are eligible for the following sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year. Co-Ops and Interns are eligible to participate in the Company's consolidated retirement plan (pension). For additional general information on Company benefits, please go to: ********************************************* This job posting is anticipated to close on 09/11/2026. The Company may however extend this time-period, in which case the posting will remain available on *************************** to accept additional applications.

Role Overview & Key Functions: If you want to do something that matters, this work matters. Patients drive our passion to pioneer novel cancer therapies. That's why we've built an environment centered around support, flexibility, and a shared mission. Creating and delivering medicine for cancer can only be done through focus, dedication, and heart. We hire exceptional people and trust each other to work in whatever way lets us, be us - whether that's onsite, from home, or anywhere in between. Our summer intern program, which will run from May 25th - Aug 7th, allows students to gain real world work experience in a high energy, collaborative work culture. Role Overview & Key functions: We are seeking a motivated and detail-oriented Analytical Data Analyst Summer Intern to be part of our Analytical team. This internship offers hands-on experience in analytical data analysis, trending, and generating reports/dashboards to support business decision-making. This experience will enhance the Intern's career prospects in Analytical and related fields. Transfer data between Smartsheet and excel worksheets/workbooks. Ensuring data integrity and correct formatting in the new destination file. Develop complex spreadsheets including creating formulas, functions, PivotTables, Power Query, and data visualization tools to generate reports/dashboards for reporting metrics to be used for annual Quality Management Review (QMR) of XPOVIO products. Improve filtering techniques for data queries. Participate and collaborate in cross-functional meetings with Quality and Pharmaceutical Sciences to understand data requirements and deliver analytical support. Perform administrative tasks related to documentation to standardize formats, ensuring version control and gap assessments for missing values or duplicates as needed. Candidate Profile & Qualifications Enrolled in a full-time pharmaceutical science, or statistical degree program Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams Proficiency with PowerBI, JMP or excel statistical add-on packages a plus Strong organization skills with the ability to handle multiple projects simultaneously and effectively Strong communication and time management skills capable of working independently and cross-functionally in a remote work environment Familiar with data analytics and trending including excel for graphing and hyperlinking source documents Analytical or quality control experience in small or large molecules or oral drug products a plus for exposure to different types of data Interest in understanding FDA regulatory commitments in commercial programs Familiar with cGMP, USP, FDA, and ICH requirements a plus You have a strong interest in life sciences and are passionate about giving patients with cancer a chance to enjoy more of life's precious moments. You feel a strong connection with our ICARE values (Innovation, Courage, Alignment & Accountability, Resilience, and Energy) You demonstrate enthusiasm for learnin Candidate Profile & Requirements: Must be able to complete the Karyopharm Internship Program 27 May - 08 Aug 2025 Currently enrolled high school or college (bachelor's program) student Student must be returning to school in the Fall Term. Must have a minimum GPA of 3.0 Must be highly organized and have the ability to work in independently and collaboratively as a team Clear, concise verbal & written communication Pay for internships ranges from $22 to $30 per hour, depending on the student's academic level (e.g., Bachelor's, Master's) and year in school. Our Value Proposition: At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* **Job Function:** Career Programs **Job Sub** **Function:** Non-LDP Intern/Co-Op **Job Category:** Career Program **All Job Posting Locations:** Danvers, Massachusetts, United States of America **Job Description:** Johnson & Johnson is currently seeking a **Product Development Co-op** to join our **ECP Advance Development Team** located in **Danvers, MA** . At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/ (******************************************************************************* . **Program Dates:** January 12 - June 26, 2026 **Position Summary** _The Advance Development (AD) team within the ECP platform is a multi-disciplinary group focused on exploring and validating innovative concepts at the earliest stages of product development. The team rapidly prototype, and evaluate feasibility of new technologies. By uncovering risks and challenges early, the AD team helps accelerate innovation while minimizing surprises before projects move into later development phases. This co-op position offers hands-on exposure to early-stage medical device innovation, where creativity, problem solving, and multi-functional collaboration are key to success._ **Key Responsibilities** + _Assist with CAD Designing, prototyping, assembly, and bench testing of early-stage device concepts._ + _Support testing, data collection, and analysis to evaluate technical feasibility._ + _Document results and contribute to technical reports and presentations._ + _Collaborate with multi-functional team members to address design and testing challenges._ + _Participate in project planning and risk assessment activities._ **Minimum Requirements** + _Pursuing a degree in Biomedical Engineering, Mechanical Engineering, or related subject areas._ + _Hands-on experience with prototyping, lab testing, or mechanical/electrical systems._ + _Familiarity with CAD tools (e.g., SolidWorks) and data analysis tools (Excel, MATLAB, or similar)._ + _Detail oriented, Strong problem-solving, analytical, and organizational skills._ + _Ability to work independently and collaboratively within a multi-functional team._ + _Strong written and verbal communication skills._ Permanently authorized to work in the U.S., must 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 requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. _Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via_ _*******************/contact-us/careers_ _. Internal employees contact AskGS to be directed to your accommodation resource._ **Required Skills:** **Preferred Skills:** **The anticipated base pay range for this position is :** 23$ per hour to 51.50$ per hour Additional Description for Pay Transparency: The anticipated base pay for this position is between 23$ per hour and 51.50$ per hour but will be based on candidate's program year, discipline, degree and/or experience. This position is overtime eligible. Intern/Co-ops may be eligible to participate in Company employee benefit programs such as medical insurance, sick time, holiday pay, and the Company's consolidated retirement plan in accordance with the terms of the applicable plans. Housing stipend will be offered for those that qualify. This position is ineligible for severance. For additional general information on Company benefits, please go to: *********************************************

Job Title: mRNA Analytical Sciences - Vaccines Summer-Fall Co-op About the Job Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you'll help advance prevention on a global scale - and shape the future of immunization. At Sanofi, we chase the miracles of science, and we know mRNA has a role to play in the future of health. And while the pandemic has shaken up our industry, creating new opportunities and risks, we believe the acceleration of innovation with mRNA technology means vaccines and treatments for more people faster than before. That's why we're looking for bold, optimistic world-changers to join our mRNA Center of Excellence. We're investing €400m a year into the new Center, hiring a team of 450 dedicated employees, and focusing on implementing an integrated end-to-end mRNA vaccine capabilities and research platform with R&D, digital and CMC teams. Bring your ambition and optimism and join us on our journey to discover and deliver transformative medicine to patients through the advancement of our cutting-edge mRNA technology! As an mRNA co-op student in Analytical Sciences, you will ensure laboratory activities in support of process development and industrialization and ensure the characterizations of mRNA vaccines in development. 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. Main Responsibilities: In this position you may perform the following duties: Perform mRNA vaccine analytical testing in the lab, data analysis, and related document writing with a critical look at the relevance of the results. Perform sample preparation following existing SOPs or analytical procedures. Perform Western blot development, optimization, qualification, and testing. Perform mammalian cell culture and transfections. Perform ELISA development, optimization, and testing Perform Flow cytometry and dd PCR testing Perform data analysis, and related document writing with a critical look at the relevance of the results. Develop and write work plans/protocols. Summarize and communicate the progress of your work. Participate in laboratory automation to set up high-throughput analyses. Accompany and train newcomers in analytical technologies and methods. Participate laboratory organization activities (orders, management/maintenance of equipment, reception & verification of reagents and receipt of samples). Compliant to Sanofi Quality standards and HSE policy. Participate in continuous improvement of laboratory safety and quality compliance. About You Basic Qualifications: Currently enrolled and pursuing a PhD in biology, biochemistry, or biotechnology or related field with the expectation that you will complete your current degree by the Spring of 2029. 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-Friday, for the full duration of the co-op/internship Practical experience or knowledge of some of the biological and biochemical analytical techniques (Western blot, cell culture, transfections, ELISA, qPCR, dd PCR, flow cytometry, and others...) Hands-on experience with mammalian cell culture Hands-on experience in high-throughput automation Interest in digital transformation and automation 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 requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship Preferred Qualifications: Good professional writing skills Essential qualities include ability to work in a fast paced, matrix environment; agility to respond to urgent requests, and initiative to lead new tasks. Adherence to Quality and HSE aspects. Why Choose Us: Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Exposure to cutting-edge technologies and research methodologies. Networking opportunities within Sanofi and the broader biotech community. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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. #GD-SP #LI-SP #LI-Onsite #vhd #mRNA 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. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! US and Puerto Rico Residents Only Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The U.S. CSR & Philanthropy team at Takeda leads strategic initiatives that foster meaningful community engagement and social impact. Through philanthropic giving, volunteerism and corporate giving, the team supports Takeda's commitment to corporate social responsibility. As part of the broader U.S. Community Health team in Takeda's U.S. Public Affairs organization, CSR & Philanthropy plays a key role in amplifying Takeda's values-driven mission and strengthening connections with local communities. As the Community Engagement Intern, you will play a key role in advancing Takeda's commitment to social impact and employee engagement. This internship offers hands-on experience in corporate social responsibility, with opportunities to support philanthropic giving, volunteerism, and internal communications that connect employees to meaningful community initiatives. The role may also offer exposure to other areas within Takeda's U.S. Public Affairs organization, providing broader insight into how the company engages with external stakeholders and communities. How You Will Contribute: As the Community Engagement Intern, you will have the opportunity to… Support Takeda's U.S. volunteerism efforts through project coordination, employee communications and logistical planning for both on-site and off-site activities. Develop internal and external communications to promote employee engagement and philanthropic initiatives across multiple channels (e.g., newsletters, SharePoint, Viva Engage, digital signage, social media). Administer the volunteerism and giving platform to manage matching gift requests, volunteer time submissions and project registration and to track participation metrics. Attend meetings with nonprofit partners to observe program updates, learn about community impact, and gain insight into how Takeda builds and maintains strategic philanthropic relationships. Participate in internal team meetings and events. Lead or assist with ad hoc projects as needed. Internship Development Opportunities: Gain hands-on experience in corporate social responsibility and community engagement. Build communication and project management skills in a professional setting. Learn how philanthropic programs are structured and evaluated within a global organization. Network with professionals across Takeda through team meetings and planned events. Strengthen your ability to work independently and collaboratively in a hybrid work environment. Job Requirements: This position will be hybrid out of Takeda's Cambridge, MA location (Kendall Square). Must be pursuing a Bachelor's degree in CSR, Communications, Marketing, Public Relations, Political Science, or other social sciences. Strong organizational, planning, and deadline-driven skills. Analytical and problem-solving abilities. Self-motivated, adaptable and able to work both independently and in teams. Excellent written and verbal communication skills. Proficiency in Microsoft Office Suite. Internship Eligibility Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship Must be currently enrolled in a degree program graduating December 2026 or later The internship program is 10-12 weeks depending on the two start dates (May 26th-August 14th or June 15th- August 21st) The intern must be able to commit to one of these time frames Able to work full time 40 hours a week during internship dates Takeda does not provide a housing stipend or relocation support for the U.S Summer Internship Program Program Highlights: Hands-on experience with real projects and responsibilities Dedicated mentorship program pairing interns with experienced professionals Networking opportunities with industry professionals and fellow interns Internship events focused on professional and skills development Exposure to multiple business areas or departments within a Pharmaceutical Organization Applications will be accepted between October 31st- November 16th Takeda Compensation and Benefits Summary We understand compensation may be an important factor as you consider an internship opportunity. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - MA - Cambridge - Kendall Square - 500 U.S. Hourly Wage Range: $21.00 - $46.00 The estimated hourly range reflects an anticipated range for this position. The actual hourly wage offered will depend on the candidate's school year/level to be entered following completion of internship. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. internship benefits vary by location and may include: Paid sick time Civic Duty paid time off Participation at company volunteer events Participation at company sponsored special events Access to on-site fitness center (where available) Commuter Benefit: To offset your work-commute expenses, Takeda provides U.S. employees with a fixed monthly subsidy to be used for either public transportation (transit) or parking. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. LocationsUSA - MA - Cambridge - Kendall Square - 500Worker TypeEmployeeWorker Sub-TypePaid Intern (Fixed Term) (Trainee) Time TypeFull time Job Exempt NoIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

We are looking for Junior and Master's Level students studying Biomedical Engineering, Biotechnology, or a related field for a 10-week internship role at our Alexion: AstraZeneca Rare Disease site in Cambridge, MA from June 1 2026 to August 07 2026. Position Description: Design and execute studies to support the ongoing process development for selected program(s) Participate in lab organization/workflow improvement initiatives Complete relevant documentation (production records, data analysis etc) Position Requirements: Junior and Master's Level students studying Biomedical Engineering, Biotechnology, or a related field Candidates must have an expected graduation date after August 2026. Cell culture and aseptic technique required Transfection, Data analysis tools (GraphPad, JMP, Excel) preferred Enthusiasm for collaboration, cross-functional projects, public speaking, and presentation design. US Work Authorization is required at time of application. Ability to report onsite to Cambridge, MA 5 days per week. This role will not provide relocation assistance. Compensation range: $37-41 per hour Compensation Pay Range: The annual base pay (or hourly rate of compensation) for this position is outlined above. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Date Posted 08-Jan-2026 Closing Date 22-Jan-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice (************************************** and Terms of Use (********************************************* . I further attest that all information I submit in my employment application is true to the best of my knowledge. **Job Description** The Computational Oncology team drives innovation by transforming 'omics and biomarker data into actionable insights that accelerate Takeda's Oncology pipeline. As part of the Precision and Translational Medicine organization, we collaborate across disciplines to decode complex datasets and shape strategies for personalized cancer therapies. Our mission is to improve patient outcomes by integrating cutting-edge analytics with translational science in a dynamic, purpose-driven environment. In this role, the candidate will collaborate with cross-functional teams to design and execute independent analyses using proprietary tumor datasets. They will integrate gene expression, protein abundance, and genetic mutation data to support precision medicine strategies. This hands-on experience offers the opportunity to contribute to personalized cancer treatment and make a meaningful impact on patient outcomes in a highly collaborative and innovative setting. **How You Will Contribute:** + Collaborate with scientists across oncology, bioinformatics, and translational medicine, contributing to cross-functional research initiatives and gaining exposure to diverse perspectives in cancer research. + Develop and apply innovative methods for integrating and analyzing multi-omics tumor data, using approaches such as statistical modeling and machine learning to uncover novel insights. + Combine proprietary datasets with known biological pathways, networks, and interactions to explore mechanisms of treatment response and resistance. + Identify molecular subtypes of cancers to support precision medicine strategies, including patient stratification and biomarker discovery. + Design and execute your own integrative multi-omics analysis, tailored to your interests and experience, with guidance from experienced mentors. **Internship Development Opportunities:** + Gain hands-on experience applying bioinformatics skills to high-quality proprietary datasets, contributing to real-world oncology research. + Learn about the Oncology drug development process and discover how computational biology informs key decisions in precision medicine. + Engage with leading industry professionals, gaining insights into the impact of your work and exploring career paths in translational science and the pharmaceutical industry. **Job Requirements:** + This position will be **Hybrid (1-3 days/week in office)** out of the **Cambridge, MA** location + Must be pursuing a **Doctoral** Degree in Computational Biology, Bioinformatics, Computer Science, or a related field + Strong foundation in biology, chemistry, biochemistry, biostatistics, or a related scientific field + Hands-on experience or coursework in bioinformatics, with exposure to transcriptomics, proteomics, or genetic mutation analysis + Proficiency in R + Interest in applying 'omics data to real-world healthcare and drug development challenges + Clear and effective communication skills, with the ability to work well in cross-functional teams + Strong analytical thinking and problem-solving abilities + Ability to write clean, reproducible code and document analyses for collaborative research **Internship Eligibility** + Must be authorized towork in the U.S. on a permanent basis without requiring sponsorship + Must be currently enrolled in a degree program graduating December 2026or later + The internship program is 10-12 weeksdepending on the two start dates (May 26th-August 14thor June 15th- August 21st) + The intern must be able to commit to one of thesetime frames + Able to work full time 40 hoursa week during internship dates + Takeda does not provide a housing stipend or relocation support for the U.S Summer Internship Program **Program Highlights:** + Hands-on experience with real projects and responsibilities + Dedicated mentorship program pairing interns with experienced professionals + Networking opportunities with industry professionals and fellow interns + Internship events focused on professional and skills development + Exposure to multiple business areas or departments within a Pharmaceutical Organization **Takeda Compensation and Benefits** **Summary** We understand compensation may be an important factor as you consider an internship opportunity. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. **For Location:** Boston, MA **U.S. Hourly Wage Range:** $21.00 - $46.00 The estimated hourly range reflects an anticipated range for this position. The actual hourly wage offered will depend on the candidate's school year/level to be entered following completion of internship. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. internship benefits vary by location and may include: + Paid sick time + Civic Duty paid time off + Participation at company volunteer events + Participation at company sponsored special events + Access to on-site fitness center (where available) + Commuter Benefit: To offset your work-commute expenses, Takeda provides U.S. employees with a fixed monthly subsidy to be used for either public transportation (transit) or parking. **EEO Statement** _Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law._ **Locations** Boston, MA **Worker Type** Employee **Worker Sub-Type** Paid Intern (Fixed Term) (Trainee) **Time Type** Full time **Job Exempt** No It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

About the Job Sanofi is committed to becoming a leader in immunology with over 10 mid and late-stage clinical assets being studied across several immunological disease areas. The New Product Launch team was recently created to support the early commercial planning for this promising pipeline and to help prepare the company and the market for these new, potential treatment options for patients suffering from immunological diseases in the fields of dermatology, respiratory, rheumatology and gastroenterology. We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. Main Responsibilities: The New Product Launch (NPL) Summer Intern will report to a Senior Director within the NPL team to assist with one or more of the following projects: * Work with the global brand teams and NPL commercial team to support the development of a preliminary US Brand Plan for any of our late-stage clinical assets, including rilzabrutinib and duvakitug * Complete a competitor analysis within at least one of the following therapeutic areas: asthma / chronic spontaneous urticaria (CSU) / IgG4-related disease (IgG4-RD) / ulcerative colitis / Crohn's Disease to evaluate and summarize current treatments and existing competitors already in the space, therapies in development, and available resources and patient support programs * Support market access assessment and early forecasting efforts to scenario plan various launch strategies * Participate in market research projects and help identify any insights gaps for future planning About You Basic Qualifications: * Currently enrolled and pursuing an MBA at an accredited college or university with the expectation that you will complete your current degree in the Spring of 2027 * Must have completed the first year of your MBA program prior to the summer internship * Must be enrolled in school the throughout the full duration of the internship with Sanofi * Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship * 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 requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship Preferred Qualifications: * Desire to serve patients, passion for the patient * Excellent communication skills, interpersonally savvy, ability to collaborate across boundaries * Strong analytical skills, ability to package and present strategic insights and learning * Highly organized with the ability to effectively manage multiple projects and priorities Why Choose Us? * Bring the miracles of science to life alongside a supportive, future-focused team. * Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. * Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. * Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave. * Exposure to cutting-edge technologies and research methodologies. * Networking opportunities within Sanofi and the broader biotech community. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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. #GD-SG #LI-GZ #LI-Onsite #vhd 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. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! US and Puerto Rico Residents Only Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.

About the Job Sanofi is committed to becoming a leader in immunology with over 10 mid and late-stage clinical assets being studied across several immunological disease areas. The New Product Launch team was recently created to support the early commercial planning for this promising pipeline and to help prepare the company and the market for these new, potential treatment options for patients suffering from immunological diseases in the fields of dermatology, respiratory, rheumatology and gastroenterology. We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. Main Responsibilities: The New Product Launch (NPL) Summer Intern will report to a Senior Director within the NPL team to assist with one or more of the following projects: Work with the global brand teams and NPL commercial team to support the development of a preliminary US Brand Plan for any of our late-stage clinical assets, including rilzabrutinib and duvakitug Complete a competitor analysis within at least one of the following therapeutic areas: asthma / chronic spontaneous urticaria (CSU) / IgG4-related disease (IgG4-RD) / ulcerative colitis / Crohn's Disease to evaluate and summarize current treatments and existing competitors already in the space, therapies in development, and available resources and patient support programs Support market access assessment and early forecasting efforts to scenario plan various launch strategies Participate in market research projects and help identify any insights gaps for future planning About You Basic Qualifications: Currently enrolled and pursuing an MBA at an accredited college or university with the expectation that you will complete your current degree in the Spring of 2027 Must have completed the first year of your MBA program prior to the summer internship Must be enrolled in school the throughout the full duration of the internship with Sanofi Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship 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 requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship Preferred Qualifications: Desire to serve patients, passion for the patient Excellent communication skills, interpersonally savvy, ability to collaborate across boundaries Strong analytical skills, ability to package and present strategic insights and learning Highly organized with the ability to effectively manage multiple projects and priorities Why Choose Us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave. Exposure to cutting-edge technologies and research methodologies. Networking opportunities within Sanofi and the broader biotech community. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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. #GD-SG #LI-GZ #LI-Onsite #vhd 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. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! US and Puerto Rico Residents Only Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.

The Ceramic Studio Youth Classes Internship program is a great opportunity for aspiring ceramic artists with a passion for working with youth to gain access to an educational ceramic studio, granting exposure to many aspects of studio operations and providing a path for educational growth as well as studio access in return for scheduled work shifts. Interns are expected to make a commitment of no less than one semester/season of participation. Interns should be at least 18 years old, exceptions may be made if the applicant has several years of ceramics experience. Preference will be given to applicants that are able to make a 2-semester commitment Winter 2026 (January - March) & Spring 2026 (April - June). More information

We are looking for doctoral level students majoring in Computational Biology, Bioinformatics, Systems Biology, Biomedical Informatics (with a specialization in AI, ML, or genomics) or a related discipline for a 10-week internship role in Waltham, MA from June 1st to August 7th. Position Duties: Design and Build the Agentic Framework: Lead the design, rapid prototyping, and testing of a multi-agent AI system using Python and modern LLM/agentic frameworks (e.g., LangChain, AutoGen, Google ADK or similar). Infuse and Validate Biological Domain Knowledge: Act as the "subject matter expert" to guide the AI. You will apply your deep knowledge of oncology/immunology to curate training data, design prompts for hypothesis generation, and critically evaluate the AI's outputs. Integrate and Demonstrate Pipelines: Integrate the separate agents into a single, end-to-end proof-of-concept pipeline constructing. Position Requirements: Doctoral level students majoring in Computational Biology, Bioinformatics, Systems Biology, Biomedical Informatics (with a specialization in AI, ML, or genomics) or a related discipline. Candidates must have an expected graduation date after August 2026. High-Dimensional Genomics Data Handling: Proven experience in cleaning, preprocessing, and analyzing large biological datasets, such as RNA-seq, sc RNA-seq, proteomics, or genomic data, is required. Coding Proficiency: Coding skills in R and Python, including libraries for scientific computing (NumPy, Pandas), are required. Agentic Frameworks & LLMs: Direct, hands-on experience with orchestration frameworks like LangChain, AutoGen, CrewAI, or similar tools used for building multi-agent systems and leveraging Large Language Models (LLMs) is required. Oncology/Immunology: Specific experience or coursework focused on molecular pathways, disease mechanisms, and the interpretation of gene expression data are a plus. Deep Learning/ML Expertise: Experience with deep learning frameworks like PyTorch or TensorFlow is a plus. Ability to report onsite to Waltham, MA 3-5 days per week. This role will not provide relocation assistance. US Work Authorization is required at time of application. This role will not be providing OPT support. Compensation: $48 hourly Date Posted 17-Dec-2025 Closing Date 15-Jan-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: Career Programs Job Sub Function: Non-LDP Intern/Co-Op Job Category: Career Program All Job Posting Locations: Danvers, Massachusetts, United States of America Job Description: Johnson & Johnson is currently seeking a Product Development Co-op to join our ECP Advance Development Team located in Danvers, MA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/. Program Dates: January 12 - June 26, 2026 Position Summary The Advance Development (AD) team within the ECP platform is a multi-disciplinary group focused on exploring and validating innovative concepts at the earliest stages of product development. The team rapidly prototype, and evaluate feasibility of new technologies. By uncovering risks and challenges early, the AD team helps accelerate innovation while minimizing surprises before projects move into later development phases. This co-op position offers hands-on exposure to early-stage medical device innovation, where creativity, problem solving, and multi-functional collaboration are key to success. Key Responsibilities * Assist with CAD Designing, prototyping, assembly, and bench testing of early-stage device concepts. * Support testing, data collection, and analysis to evaluate technical feasibility. * Document results and contribute to technical reports and presentations. * Collaborate with multi-functional team members to address design and testing challenges. * Participate in project planning and risk assessment activities. Minimum Requirements * Pursuing a degree in Biomedical Engineering, Mechanical Engineering, or related subject areas. * Hands-on experience with prototyping, lab testing, or mechanical/electrical systems. * Familiarity with CAD tools (e.g., SolidWorks) and data analysis tools (Excel, MATLAB, or similar). * Detail oriented, Strong problem-solving, analytical, and organizational skills. * Ability to work independently and collaboratively within a multi-functional team. * Strong written and verbal communication skills. Permanently authorized to work in the U.S., must 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 requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers . Internal employees contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: The anticipated base pay range for this position is : 23$ per hour to 51.50$ per hour Additional Description for Pay Transparency: The anticipated base pay for this position is between 23$ per hour and 51.50$ per hour but will be based on candidate's program year, discipline, degree and/or experience. This position is overtime eligible. Intern/Co-ops may be eligible to participate in Company employee benefit programs such as medical insurance, sick time, holiday pay, and the Company's consolidated retirement plan in accordance with the terms of the applicable plans. Housing stipend will be offered for those that qualify. This position is ineligible for severance. For additional general information on Company benefits, please go to: *********************************************

Role Overview & Key Functions: If you want to do something that matters, this work matters. Patients drive our passion to pioneer novel cancer therapies. That's why we've built an environment centered around support, flexibility, and a shared mission. Creating and delivering medicine for cancer can only be done through focus, dedication, and heart. We hire exceptional people and trust each other to work in whatever way lets us, be us - whether that's onsite, from home, or anywhere in between. Our summer intern program, which will run from May 25th - Aug 7th, allows students to gain real world work experience in a high energy, collaborative work culture. Role Overview & Key functions: We are seeking a motivated and detail-oriented Analytical Data Analyst Summer Intern to be part of our Analytical team. This internship offers hands-on experience in analytical data analysis, trending, and generating reports/dashboards to support business decision-making. This experience will enhance the Intern's career prospects in Analytical and related fields. * Transfer data between Smartsheet and excel worksheets/workbooks. Ensuring data integrity and correct formatting in the new destination file. * Develop complex spreadsheets including creating formulas, functions, PivotTables, Power Query, and data visualization tools to generate reports/dashboards for reporting metrics to be used for annual Quality Management Review (QMR) of XPOVIO products. * Improve filtering techniques for data queries. * Participate and collaborate in cross-functional meetings with Quality and Pharmaceutical Sciences to understand data requirements and deliver analytical support. * Perform administrative tasks related to documentation to standardize formats, ensuring version control and gap assessments for missing values or duplicates as needed. Candidate Profile & Qualifications * Enrolled in a full-time pharmaceutical science, or statistical degree program * Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams * Proficiency with PowerBI, JMP or excel statistical add-on packages a plus * Strong organization skills with the ability to handle multiple projects simultaneously and effectively * Strong communication and time management skills capable of working independently and cross-functionally in a remote work environment * Familiar with data analytics and trending including excel for graphing and hyperlinking source documents * Analytical or quality control experience in small or large molecules or oral drug products a plus for exposure to different types of data * Interest in understanding FDA regulatory commitments in commercial programs * Familiar with cGMP, USP, FDA, and ICH requirements a plus * You have a strong interest in life sciences and are passionate about giving patients with cancer a chance to enjoy more of life's precious moments. * You feel a strong connection with our ICARE values (Innovation, Courage, Alignment & Accountability, Resilience, and Energy) * You demonstrate enthusiasm for learnin Candidate Profile & Requirements: * Must be able to complete the Karyopharm Internship Program 27 May - 08 Aug 2025 * Currently enrolled high school or college (bachelor's program) student * Student must be returning to school in the Fall Term. * Must have a minimum GPA of 3.0 * Must be highly organized and have the ability to work in independently and collaboratively as a team * Clear, concise verbal & written communication Pay for internships ranges from $22 to $30 per hour, depending on the student's academic level (e.g., Bachelor's, Master's) and year in school. Our Value Proposition: At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!