Programming Intern

Descrizione del lavoro:

At Genmab, we are dedicated to building extra[not]ordinary® 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 company's 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 we're always looking for smart, purpose-led candidates to play a role in our bold, extra[not]ordinary® future.

Job Overview
The Intern will support Genmab's 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 patterns-such as state license formatting inconsistencies, physician relocations, and name changes-and 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 You'll 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 Bachelor's or Master's 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.

What's 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 it's important to complete all relevant questions to ensure we have as much information about you as possible.

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

If you move forward in the process, you'll 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 you'll 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 you're 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, Genmab's 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 Genmab.com 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 (genmab.com)