This is an internship role for a Project Manager in Marketing and Market Access in the healthcare sector. The role involves contributing to the design, structuring, and deployment of support offers for healthcare establishments, supporting field teams, and implementing marketing and event actions. The ideal candidate is a Master's student with strong project management skills, an appetite for market access and healthcare challenges, and good analytical and synthesis abilities.

Alternating student in Analytical Chemistry - Analytical Support (H/F) for a 12-month duration, based in Igoville, starting September 2026. The role involves developing and validating new analytical methods for quality control of raw materials and finished products, with a focus on chromatography techniques. The position is within the pharmaceutical industry and requires adherence to quality standards (GMP, FDA) and safety regulations.

This role is a Production Operator in a Fill/Finish facility, responsible for executing and monitoring production processes from material loading to finished product packaging, ensuring adherence to quality standards, safety regulations, and GMP guidelines. The position requires basic understanding of GMP and safety, at least one year of industrial manufacturing experience (preferably in pharmaceuticals), and the ability to work under pressure and perform physical tasks.

This role is for a Clinical Director (Principal Scientist) in Translational Medicine, focusing on the early clinical development of novel therapeutics within Immunology. The position involves leadership in designing and executing clinical development strategies, developing biomarker strategies, contributing to target identification, and providing clinical pharmacology support. The role requires an MD or MD/PhD with a strong background in basic and/or clinical translational research, a proven track record in clinical medicine or research, and a demonstrated record of scientific scholarship.

This role focuses on establishing and governing a trusted enterprise data foundation across the Veeva platform. Key responsibilities include defining and enforcing data standards, quality controls, and lineage, as well as shaping governed data products. The goal is to enable compliance, automation, and AI readiness by ensuring data integrity and accessibility across various vaults and cross-domain workflows.

This is an internship role for a Digital Project Management Assistant at Merck, focusing on the development, launch, and maintenance of digital services for healthcare professionals. Responsibilities include SEO optimization, conversion rate optimization (CRO), data analysis for site hygiene, operational management of digital services, and testing/quality assurance. The role involves collaborating with various cross-functional teams.

This role focuses on supporting and facilitating learning and development activities within the FLSL/SLSL commercial and compliance sectors of Merck's pharmaceutical business. The Senior Training Manager will collaborate with business leaders to understand needs, design and execute learning plans, and ensure successful learning outcomes. The role involves consulting, delivery of training, and acting as a liaison between the L&D function and business units to drive desired business results through enhanced capabilities.

The Regional Medical Scientific Director (RMSD) is a therapeutic and disease expert responsible for bidirectional scientific and medical information exchange with Scientific Leaders (SLs). This role involves engaging with SLs to provide balanced, factual information about non-product areas and Company products, supporting scientific exchange, research initiatives, scientific congresses, and gathering scientific insights. The RMSD acts as a liaison between the scientific community and the Company, enhancing understanding of scientific foundations and goals for trials and research studies. Key responsibilities include developing relationships with SLs, conducting scientific discussions, addressing scientific questions, maintaining knowledge of the therapeutic area, initiating discussions for research strategies, identifying barriers to patient enrollment, recommending study sites, and supporting clinical development programs. The role also involves gathering feedback to understand medical or scientific needs and priorities.

The Regional Medical Scientific Director (RMSD) is a credentialed therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies. The RMSD serves as a role model for other field medical team members in ways that include on-boarding and/or sharing of therapeutic expertise.

The Regional Medical Scientific Director is a therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.

This role is for a Regional Medical Scientific Director in Ophthalmology at Merck. The primary focus is on scientific and medical information exchange with Scientific Leaders, supporting research initiatives, and gathering scientific insights within the therapeutic area. The role requires deep therapeutic expertise and engagement with the scientific community regarding approved and investigational products and trials.

This role is for an Clinical Operations Project Manager intern at Merck, focusing on supporting clinical trial operations, regulatory submissions, and logistical aspects within the pharmaceutical industry. The position involves cross-functional collaboration with regulatory affairs and pharmacovigilance teams, managing trial documentation, and ensuring compliance with regulations like EU No 536/2014. It is not directly involved in AI/ML development.

This is an internship role for a Pediatric Vaccines Product Manager Assistant at Merck. The role involves supporting product managers in executing the marketing plan for pediatric vaccines, creating and implementing marketing campaigns across various channels, developing promotional tools, organizing sales force seminars and external events, and conducting market research and competitor analysis. The ideal candidate is in their final year of business school or a scientific degree with a marketing specialization.

This is an internship position for a Clinical Research Associate (Attaché de Recherche Clinique) at Merck, focusing on supporting the monitoring of clinical trials in France. The role involves administrative support, remote monitoring, and gaining field experience in clinical site monitoring. It requires knowledge of the regulatory framework for clinical trials and strong organizational skills.

This is an internship position for a Regulatory Affairs Officer focusing on drug regulations within the French subsidiary of a pharmaceutical company. The role involves supporting the regulatory team in various tasks such as dossier submissions, monitoring evaluations by health authorities, controlling packaging and labeling, and participating in regulatory intelligence.

This is an internship role for a Project Coordinator in CRM at Merck, focusing on administering, testing, and supporting CRM tools, as well as data analysis and user training. The role is within the Digital Marketing Operations team and requires a Master's student with strong Excel and PowerBI skills, good communication, and an understanding of the pharmaceutical business.

Internship role supporting a Medical Affairs team at Merck, focusing on program execution, literature review, data analysis, regulatory compliance, cross-functional collaboration, scientific material development, and administrative tasks. The role involves contributing to medical research projects and staying updated on medical developments.

This role is responsible for embedding ethical business conduct and regulatory adherence across Human Health International (HHI) within Vietnam. It ensures local operations align with global standards, regional frameworks, and country-specific laws, acting as a trusted advisor to country leadership to enable compliant business growth and foster a culture of integrity, transparency, and accountability. Key responsibilities include business practice leadership, governance and policy implementation, risk management and monitoring, training and awareness, business partnership and advisory, due diligence oversight, and reporting.

Werkstudent (m/w/d) Quality Assurance Systems role at Merck, focusing on document management, archiving, project support, and continuous improvement of quality-related processes. Requires a science or comparable degree, strong MS Office skills, structured work style, initiative, and good communication in German and English.

This role at Merck focuses on medical affairs within oncology, involving the design, planning, and execution of medical research, development of country medical affairs plans, and engagement with scientific leaders. It requires clinical and research experience in healthcare, knowledge of pharmaceutical regulations, and experience with scientific publications or presentations. The role emphasizes strategic thinking, scientific communication, and fostering collaboration within a global context.

This role is a Senior Specialist in R&D Clinical Quality Assurance at Merck, focusing on ensuring data integrity and compliance with global regulatory requirements in clinical trials across the APAC region. The primary responsibilities include conducting GCP audits, preparing audit reports, collaborating with various teams to resolve observations, and supporting the overall quality assurance processes within clinical development.

This role at Merck focuses on clinical research in oncology, involving the planning, execution, and reporting of clinical trials. The scientist will collaborate with internal and external stakeholders, including regulatory bodies, to support the global development of new oncology drugs. Responsibilities include inputting into development strategy, preparing regulatory submission documents, managing clinical trial protocols, monitoring data, and contributing to publications.

This role is for a Clinical Research Manager at Merck, focusing on leading clinical trial operations in Japan. Responsibilities include managing trial planning, execution, and closure, leading a team, managing costs and risks, and ensuring quality and compliance. The role requires strong English and Japanese language skills, and experience in clinical research management or as a Project Leader at a CRO.

Internship role focused on facility management, specifically creating an inventory and registration system for lighting fixtures. Involves platform research (Excel, SharePoint, Power Apps, Power BI), data modeling, data entry, and reporting to support asset management and replacement planning.

This is an Assistant Product Manager role in Oncology at Merck, focusing on marketing and strategic support for an immunotherapy drug. The role involves creating marketing campaigns, developing promotional tools, analyzing market data, and participating in digital marketing initiatives. It requires a background in science and business/marketing, with strong analytical and teamwork skills.

This role is for an Associate Clinical Research Manager (aCRM) in the General and Specialty Medicine/Infectious Diseases & Vaccines CRM domain at Merck, with a career path towards becoming a Clinical Research Manager (CRM). The aCRM will gain skills and knowledge in clinical trial operations under the guidance of a CRM, potentially also performing CRA duties. The CRM role involves leading clinical trial operations in Japan, collaborating with US counterparts, managing trial teams, vendors, costs, milestones, risks, and supporting site-level issue resolution.

Seeking a Sr. Manager/Associate Director for Biomarker Research in Shanghai, to drive clinical biomarker strategy and provide scientific expertise for clinical development programs. Responsibilities include developing and implementing biomarker strategies, providing scientific input to asset development teams, liaising with cross-functional teams, analyzing and interpreting results, and representing biomarker aspects internally and externally. Requires a Ph.D. in a life science field with 5+ years of experience, a track record in biomarker strategy, and broad knowledge of technical platforms like IHC, immunoassay, and NGS. Understanding of drug discovery and development is essential.

Project lead for early clinical research in China for GYN programs, focusing on developing products towards registration, engaging KOLs, and preparing for regulatory submission.

This role involves analyzing scientific literature, conducting primary research on diseases, identifying unmet medical needs, and generating reports and presentations to support drug development and asset evaluation within the pharmaceutical R&D sector. It requires strong information search and analytical skills, with a focus on preclinical and clinical data.

The Safety Data Lead role at Merck focuses on analyzing and interpreting adverse experience (AE) reports for investigational and marketed products, ensuring compliance with regulatory requirements and internal processes within Global Pharmacovigilance Case Management (GPVCM). This role involves data entry, collaboration with stakeholders, and supporting process optimization. It requires a healthcare or life sciences degree and understanding of pharmacovigilance regulations.

Responsible for processing adverse experience (AE) reports with high quality and compliance in the global safety system for investigational and/or marketed products, under the direction and supervision of a Global Pharmacovigilance Case Management Manager. Performs triage, analysis and interpretation of AE data following Company Standard Operating Procedures (SOPs) and guidelines. Supports business processes important to Global Pharmacovigilance Case Management operations and works closely with other staff within the organization as well as cross-functionally.

Senior Principal Scientist role at Merck focused on late-stage clinical research in Immunology, specifically Ophthalmology. Responsibilities include strategic planning, study design, execution, analysis, and regulatory filing for investigational compounds. Requires an MD/DO/PhD and significant experience in clinical trial design and drug development within Immunology.

The Associate Director, Product Line Lead for the Compliance product line within Merck's Information Technology division is responsible for overseeing the strategy, roadmap, development, and success of technology solutions for the Ethics & Compliance Office. This includes managing products like Privacy Management, Antibribery & Corruption, Global Trade Compliance, Policy Management, and Research Compliance. The role involves acting as a trusted partner to the business, collaborating with cross-functional teams, leading the product development lifecycle, managing a matrixed team, and ensuring products meet compliance standards and deliver measurable value. The candidate needs strong leadership, customer service, analytical, and communication skills, with experience in compliance domains and managing technology solutions.

This is an internship position for an Assistant Client Engagement Manager in the Vaccines division at Merck. The role involves supporting the development of the Vaccines Ecosystem for healthcare professionals, creating promotional materials, managing professional events, and assisting with product lifecycle management. The ideal candidate is pursuing a marketing or health-related degree with a marketing specialization, has strong communication and digital marketing skills, and is eager to gain experience in pharmaceutical marketing.

This is an apprenticeship role for a Clinical Research Manager (CRM) at Merck, focusing on the management of clinical trials in France. The role involves participating in all phases of clinical trials, from selection to closure, collaborating with various research teams, and potentially assisting with site management activities. The ideal candidate is pursuing a scientific degree with a specialization in clinical research and possesses knowledge of regulatory frameworks, project management skills, and strong communication abilities.

This is an Assistant Product Manager role in Oncology at Merck, focusing on Melanoma and Digestive Cancers. The role involves supporting marketing campaigns, creating promotional tools, analyzing market data, and contributing to digital marketing transformation. It requires a Master's degree with a dual scientific and business background, strong adaptability, creativity, rigor, teamwork, and fluent English.

This is an internship role for an Electronics Engineer focusing on Embedded Systems, specifically in the area of RFID product development and testing. The role involves R&D activities, product characterization, testing, validation, and project management within the pharmaceutical industry.

This role is for an apprentice laboratory technician in chemistry at Merck, focusing on the analysis of raw materials and finished products within Quality Control. The apprentice will evaluate and implement improvements to analysis times and processes, adhering to pharmaceutical Good Manufacturing Practices and EHS standards.

Lead day-to-day operations of an API production facility, ensuring safe, compliant, and efficient production that meets quality, budgetary, and scheduling targets. This role involves managing a multidisciplinary team, overseeing key quality subsystems, and handling financial and trade union matters within a regulated healthcare manufacturing environment.

This is an internship role for a Product Marketing Assistant in Oncology at Merck, focusing on marketing operations, promotional material creation, market research analysis, and digital marketing transformation for specific cancer therapies. The role requires a Master's degree with a dual scientific and business background.

This is an apprenticeship role for an Operational Maintenance Technician (H/F) in the pharmaceutical industry. The role involves participating in preventive and corrective maintenance on production equipment, contributing to diagnostics and troubleshooting, documenting interventions, and assisting with equipment restarts. The position also requires adherence to safety, hygiene, and quality procedures within a regulated environment.

This is an apprenticeship role for a Maintenance Technician (Technicien de Maintenance) at Merck in France. The intern will be responsible for preventive, curative, and improvement maintenance of equipment. The role requires a BAC PRO or equivalent in Maintenance or Electrical fields and emphasizes rigor, teamwork, and reactivity. The internship is for 2 years, starting September 1, 2026.

This role is for a Senior Clinical Director (Senior Principal Scientist) in Late Stage Oncology Clinical Research at Merck. The primary responsibility is planning and directing clinical research activities for new or marketed medicines, managing the entire cycle of clinical development from study design to regulatory reporting and publication. The role requires expertise in clinical medicine, drug development, and oncology research, with a focus on evaluating pre-clinical and translational work, developing clinical strategies, and overseeing clinical trials.

Internship role in Merck's In Market Quality department, focusing on quality oversight of medicine distribution in the Dutch market. Responsibilities include documentation, batch commercialization support, complaint sample management, and temperature excursion support, all within a Good Distribution Practice (GDP) framework.

Werkstudent (m/w/d) Marketing Oncology in Gastrointestinal Tumors. Responsibilities include supporting the marketing team, creating and developing advertising materials, managing approval processes, organizing events, taking on marketing projects, creating presentations, and working with MS Office. Requires a science/business degree, strong organizational skills, strategic thinking, and proficiency in MS Office and English.

Manager responsible for ensuring patient safety, high-quality data, and compliance with company requirements and regulations in clinical trials within a specific country. This role involves implementing local/global processes, identifying improvement opportunities, supporting audits and inspections, and overseeing quality control and training activities.

This role focuses on building and executing regulatory affairs strategies for new drug development in Japan, aligning with global strategies. It involves significant interaction with regulatory authorities like MHLW and PMDA, ensuring the quality of submission documents, and coordinating the preparation and submission of applications. The position requires a background in life sciences, experience in pharmaceutical development and regulatory submissions, and strong English communication skills for international coordination.

This role at Merck focuses on medical review of materials and slides, internal compliance training, and leading cross-functional projects within the Medical Affairs domain. It requires experience in pharmaceutical medical affairs or related departments, a life sciences background, and business-level English proficiency. The core responsibilities involve ensuring compliance and managing medical communications.