Novo Nordisk

Marketing

• Responsible for planning and management of all regulatory post marketing surveillance (rPMS) activities in Korea, ensuring timely, budget-compliant execution and adherence to Helsinki Declaration, ICH- Good Clinical Practice (GCP) / Good Publication Practice (GPP), Novo Nordisk Standard Operating Procedures (SOPs) and applicable law.
• Lead PMS / Post-Authorisation Safety Study (PASS) projects in the country, driving project planning, conduct and coordination from protocol outline to study reporting and being accountable for timelines and deliverables.
• Ensure compliance and quality oversight across projects, including safety reporting, monitoring recruitment/reporting status, handling protocol deviations, co-monitoring visits, audits/inspections, and vendor (Contract Research Organization), CRO) activities.
• Manage budgets, filing and archiving in the Trial Master File, update clinical trial management systems (e.g., Cosmos), and support PMS assistant in contracts and negotiation of non-interventional study agreements.
• Identify and select sites, coordinate site assessments and recruitment efforts, collaborating with line manager to ensure appropriate staffing and site allocation.
• Provide PMS / PASS related communication and insight to key internal and external stakeholders, deliver project status updates, and contribute country input to key study documents.
• Coordinate organization support in collaboration with line manager and support any local audits/inspections.

Post Marketing Surveillance Specialist

Director

• Work in close collaboration with scientific, clinical, and data-focused stakeholders
• Translate complex biological insights into clear value for projects and the broader R&D portfolio
• Drive interpretation and selection of exploratory biomarkers and omics
• Disseminate findings to inform scientific strategy
• Lead and support exploratory data-generation initiatives
• Ensure compliance with Novo Nordisk Quality Systems, Business Ethics, and HBS governance
• Author and review strategic and regulatory documents

Scientific Director – Exploratory Biomarkers, Omics

• Responsible for identifying opportunities and market potential for future CVD (cardiovascular disease) assets in Poland
• Develop and implement go-to-market strategies in alignment with global strategies
• Drive cross-functional collaboration to ensure strategic commercial perspectives are integrated into business decisions
• Lead strategic and operational initiatives to capitalize on commercial opportunities
• Build relationships with healthcare decision-makers and stakeholders to support market access and commercial success.

Cardiovascular Disease Market Development Director

Clinical Operations

• Support the day-to-day operational activities of the different clinical trials within the Global Clinical Operations team
• Collaborate with the Clinical Project Lead (CPL) and gain experience in tasks typically performed by Global Trial Managers (GTMs) and Clinical Trial Administrators (CTAs)
• Assist in coordinating trial-related documentation and tracking activities to ensure compliance with study timelines and quality standards
• Support the maintenance of trial management systems, preparing meeting materials, and contributing to the organization of investigator and vendor communications
• Help monitor study progress by reviewing operational metrics and assisting with follow-up actions as directed by the CPL
• Additional tasks may involve supporting regulatory and ethics submissions, managing essential documents, and contributing to the preparation of status reports for internal stakeholders

Intern, R&D Clinical Operations

Communications

• Work closely with experienced industry professionals and gain valuable, hands-on, full-time work experience.
• Immersed in the environment of a 24/7 commercial scale bio-production facility and contribute to the business by providing sustainable and meaningful project work.
• Get a 'behind the scenes' look at our bio-production facility as part of a project to produce photo and video content for our internal multimedia library.
• Help launch our site's internal Viva Engage Channel, and help create a post-launch engagement plan.
• Tasked with helping to coordinate employee interviews for internal content, photo shoots, and creation of video content.
• Must enter our sterile/cleanroom areas and follow GMP processes at all times.

Communications & Multimedia Internship

Manager

• Provides customer insights (Patient, HCP, Payer, Provider, etc.) to identify and assess opportunities
• Partners with key stakeholders to develop or refine market/brand/franchise/customer strategies
• Optimizes market approach and market access strategies for the organization
• Develops and helps activate insights based on patient, HCP, and payer data
• Contributes to franchise/manage markets strategic decisions
• Develops analytical models to help make business critical decisions

Market Access Insights Manager

Software Engineer

• Apply flow technology utilizing immobilized enzymes to develop the ligation reaction that is integral to our new approach to synthesis.
• Project responsibilities include the covalent immobilization of enzymes to resins, utilizing flow techniques to develop new methods for the ligation of fragments, and documenting scientific experiments.
• Specific opportunities to learn about and to utilize scientific equipment for nucleic acid synthesis and analysis techniques will be introduced.
• Techniques for immobilization, spectral determination of loading density, utilization of packed bed reactor systems for flow analysis, development of biocatalytic assays, and HPLC analysis will be applied within this project.

Biochemical Engineering Intern

Project Manager

• Work with the Nucleic Acids Project Management (NAPM) team to gain experience in Technical Project Managers
• Assist in on-boarding new project ideas and establishing early evaluation teams
• Work with scientific teams to develop project plans and timelines
• Manage stakeholders and all steps needed to mature a project through the drug discovery process
• Learn about the planning and coordination of evaluation, screening, and lead optimization stages
• Interact and learn from Nucleic Acid Project Managers, Project Vice Presidents (PVPs), and project scientists

Technical Project Management Intern

Operations

• Analyze sensor data to identify areas for optimization in laboratory automation and workflows within laboratory spaces
• Collaborate with project management and scientific stakeholders to assess equipment needs for upcoming projects (IE. new laboratory in Waltham, MA)
• Propose optimization strategies
• Maintain detailed records
• Prepare reports for stakeholders

Laboratory Operations Intern

• Work closely with experienced industry professionals for hands-on project work
• Coordinate with the global R&D legal group
• Work across a range of legal areas, including research collaborations, clinical trials, compliance, and intellectual property
• Help prioritize, staff, and execute on a variety of internal projects

Intern, Project Management

Machine Learning Engineer

• Work on the development and implementation of novel in house peptide and minibinder design platform powered by SOTA structure prediction models and enhanced sampling methods
• Integrate other enhanced sampling currently not in the pipeline such as Monte Carlo tree search
• Integrate various machine learning property predictors into the pipeline
• Benchmark NovoBind on diverse systems and improve the pipeline scope
• Implement reinforcement learning to bias the generation of designs
• Learn about state of the art structure predictors and metric, computational sequence-based binder design, reinforcement learning, drug design with computational chemistry across a broad set of modalities at Novo Nordisk including peptides, minibinders, and antibodies.

Machine Learning Intern

Data Scientist

• Work closely with experienced industry professionals and gain valuable hands-on work experience
• Analyze/visualize and/or develop algorithms on wearable and digital devices data
• Develop Python code for signal processing, AI and machine learning algorithms
• Analyze and visualize data related to wearable devices and time series signals
• Participate in regular team meetings and collaborate with the team on project work

Data Science Intern

Compliance

• own regulatory strategy and safety oversight for assigned products and projects
• lead regulatory submissions and approvals- prepare, product registrations and amendments, and respond to health authority queries
• ensure compliance and governance- maintain adherence to global and local regulatory standards, conduct reviews and audits, and manage compliance risks
• oversee pharmacovigilance activities: supervise collection, analysis and reporting of safety data, identify new safety signals and ensure timely regulatory reporting
• collaborate with stakeholders, partner with clinical, safety, commercial and external partners, and act as the company’s regulatory and safety contact for health authorities and policymakers
• monitor regulatory trends and adapt strategy, track regulatory changes, assess impact, and develop approaches to maintain compliance and accelerate approvals

Regulatory Affairs Lead – Levant

Learning and Development

• Deliver and execute leadership development priorities within assigned EVP/SVP areas
• Design and facilitate interventions using sparring, facilitation, coaching, and consultation
• Act as the primary point of contact for designated EVP areas or geographies
• Implement global processes, development offerings, and standards locally
• Collaborate with HR Business Partners and business leaders
• Lead innovation in leadership development by identifying, piloting, and scaling new learning approaches

Senior Global Leadership Development Manager

• Create and execute a 3-5-year strategic plan for your area, aligning functional objectives with affiliate, regional, and global direction.
• Together with your team develop and lead medical strategies for brands and pre-launch phases, ensuring proactive medical guidance to all functions.
• Develop strong network with key external stakeholders, including KOLs, Health Care professionals, Industry and patient associations, academic bodies, health authorities, NHS health boards and ABPI, aimed at fostering mutually beneficial partnerships and shaping market environment.
• Provide timely and relevant regulatory input enabling efficient product launches and marketing campaigns.
• Drive scientific communication strategies, including input to clinical trials, RWE plans, and publication strategies.
• Ensure compliance with ABPI Code of Practice, Health Authority requirements (MHRA) and the European Pharmacovigilance Framework.
• Lead, coach, and develop your direct reports and the whole team.
• Foster a diverse and inclusive work environment that allows people to give their best.
• Develop talents, ensuring succession planning, and participate in cross-functional development activities.
• Represent UK in internal Medical & Science regional and global leadership forums.