Programming Intern

At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain a global workplace where individuals unique contributions are valued and drive innovative solutions to meet the needs of our patients care partners families and employees.

Our people are compassionate candid and purposeful and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes our work is incredibly serious and impactful but we have big ambitions bring a ton of care to pursuing them and have a lot of fun while doing so.

Does this inspire you and feel like a fit Then we would love to have you join us!

Job Title

Programming Intern

Why Genmab

Our internship program provides interns with hands-on experience and relevant projects that directly align with our companys goals. Additionally we believe our program provides a valuable opportunity to learn thrive and build a strong network. We encourage you to review our website to learn why were always looking for smart purpose-led candidates to play a role in our bold extranotordinary future.

Job Overview

The Intern will support Genmabs compliance and data quality initiatives by contributing to the automation and analysis of CMS data validation processes. During this internship the intern will gain hands-on experience analyzing validation and matching errors related to recipient and provider demographics including NPI state license taxonomy names and addresses.

The role involves identifying common data mismatch patternssuch as state license formatting inconsistencies physician relocations and name changesand tracking gaps in CMS-validated physician reference data particularly for new or recently updated providers. The intern will also help detect late-stage defects that pass internal validation checks but fail during CMS submission and provide insights into external data dependency issues (e.g. CMS and NPI datasets) that impact submission success rates.

Working closely with cross-functional teams across data compliance and IT the intern will contribute to real-world automation efforts reporting enhancements and a capstone project that delivers measurable improvements in submission accuracy and operational efficiency

What Youll Do

• Design and build automation solutions and dashboards using the Microsoft Power Platform including Power Apps Power Automate and Dataverse/SharePoint.

• Develop validation and matching logic to identify and flag provider demographic mismatches and CMS submission failures (e.g. NPI state license taxonomy name and address).

• Create automated workflows to notify relevant stakeholders when defined thresholds or error conditions are exceeded.

• Analyze CMS submission and validation data to identify recurring error patterns and late-stage defects that impact submission success.

• Collaborate with compliance data and integration teams to understand end-to-end CMS validation workflows and external data dependencies.

• Document solution architecture automation logic dashboards and usage guidelines to support knowledge transfer and sustainability.

• Contribute to continuous improvement discussions by identifying opportunities to enhance data quality validation efficiency and operational transparency.

Required Qualifications Capabilities and Skills

• Enrollment in a Bachelors or Masters program in Computer Science Information Systems Data Science Engineering or a related field.

• Solid understanding of data validation and data quality fundamentals with the ability to identify inconsistencies in structured data.

• Hands-on experience with Microsoft Power Platform tools specifically Power Apps (Canvas apps) and Power Automate.

• Familiarity with structured data formats such as JSON and CSV.

• Basic understanding of web applications and REST API concepts.

• Experience working with SharePoint and/or Dataverse as data sources.

• Basic SQL skills for data filtering validation and trend analysis.

• Strong analytical and problem-solving skills with high attention to detail.

• Ability to work independently and collaboratively with cross-functional teams.

• Strong written and verbal communication skills including solution documentation.

Preferred Qualifications Capabilities and Skills

• Demonstrates initiative a proactive mindset and eagerness to learn in a fast-paced regulated environment.

• Experience designing or enhancing automation dashboards or workflows for data validation or operational monitoring.

• Familiarity with healthcare compliance or regulated data domains (e.g. CMS provider or reference data).

• Ability to translate business and compliance requirements into validation logic and automation workflows.

• Exposure to Python or JavaScript for scripting data processing or extending automation capabilities.

• Experience analyzing recurring data issues or trends to improve data quality and submission outcomes.

• Comfortable collaborating with compliance data and integration teams and incorporating feedback.

• Maintains strong quality standards while managing multiple tasks and priorities.

• Actively seeks feedback and applies it to continuously improve technical and professional skills

General Intern Information Date/Location/Schedule

Internships will take place June through August 2026 and be based in Princeton NJ. This role will operate on a required hybrid schedule 3 days in the office and 2 days remote per week. This role is not eligible for sponsorship.

Whats next

Help us learn about you by submitting a complete and thoughtful application which includes your resume. Your application and resume are a way for us to initially get to know you so its important to complete all relevant questions to ensure we have as much information about you as possible.

Every application matters to us and well carefully review each submission as quickly as possible to see if your qualifications align with the role. While were unable to provide individual updates rest assured that were working diligently to move through the process efficiently.

If you move forward in the process youll receive an email invitation to connect with us and dive deeper into this exciting opportunity. The final stage will bring selected candidates meeting directly with our hiring teams where youll have the chance to showcase your potential. We are committed to keeping you informed and will share decisions with all candidates as soon as we are able.

About You

• You are genuinely passionate about our purpose

• You bring precision and excellence to all that you do

• You believe in our rooted-in-science approach to problem-solving

• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds

• You take pride in enabling the best work of others on the team

• You can grapple with the unknown and be innovative

• You have experience working in a fast-growing dynamic company (or a strong desire to)

• You work hard and are not afraid to have a little fun while you do so!

Locations

Genmab maximizes the efficiency of an agile working environment when possible for the betterment of employee work-life balance. Our offices are crafted as open community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether youre in one of our office spaces or working remotely we thrive on connecting with each other to innovate.

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years its hard-working innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational quantitative and data sciences resulting in a proprietary pipeline including bispecific T-cell engagers antibody-drug conjugates next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030 Genmabs vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines.

Established in 1999 Genmab is headquartered in Copenhagen Denmark with international presence across North America Europe and Asia Pacific. For more information please visit and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice ().