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Trial Master File & Site Management Intern
Trial Master File & Site Management InternGenmab • Princeton, New Jersey, USA
Trial Master File & Site Management Intern

Trial Master File & Site Management Intern

Genmab • Princeton, New Jersey, USA
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  • [job_card.full_time]
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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

Trial Master File & Site Management 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 Trial Master File & Site Management Intern may assist various functions within the Site Management & Feasibility department. This 10-week summer internship will provide opportunities to gain skills related to clinical trial site engagement and oversight of the clinical trial master file.

Youll join a dynamic global team where youll collaborate not only with our US colleagues but also with experts from Denmark and the Netherlandsbroadening your perspective and enriching your professional experience. We believe in fostering an environment where creativity curiosity and cross-cultural collaboration are celebrated making your internship both a fun and professionally rewarding adventure.

What Youll Do

  • Ensure compliance of Trial Master File through validation and confirmation of accurate metadata
  • Review Note to File content to determine the correct TMF filing location.
  • Support with report trend and data analysis.
  • Create site performance reports using quantitative and qualitative feedback from key stakeholders
  • Research and evaluate clinical trial institutions and networks to identify unique capabilities and assess patient populations in alignment with Genmabs portfolio
  • Provide site status updates to the clinical-trial team actively participate in trial related meetings as required.
  • Oversee operational site performance e.g. site timelines enrollment compliance database lock readiness.

Required Qualifications Capabilities and Skills

  • Currently pursuing a Bachelors in Life Sciences Public Health Data Science or a related field.
  • Strong Microsoft Applications skills e.g. Word Excel and PowerPoint.
  • Strong analytical skills with experience using Excel or other spreadsheet tools for data analysis and comparison.
  • Strong computer skills and ability to learn technical applications in a fast-paced environment.
  • Strong problem-solving abilities.
  • Excellent written and verbal communication skills.
  • Ability to work independently and as part of a collaborative team.
  • High attention to detail and commitment to quality work.
  • Ability to conduct literature or database research to identify healthcare institutions networks or population data
  • Preferred Qualifications Capabilities and Skills

  • Demonstrates a global mindset with the ability to adapt communicate and collaborate effectively with team members from around the world.
  • Demonstrates an interest in artificial intelligence and innovation.
  • Demonstrates initiative a proactive attitude and eagerness to learn in a fast-paced environment.
  • Familiarity with clinical trial processes or a general understanding of regulatory documentation is a plus.
  • Comfortable synthesizing qualitative and quantitative data into clear summaries or reports.
  • General Intern Information Date / Location / Schedule

    Internships will take place June August 2026. This role will be based in our Princeton NJ office and operate on a required hybrid schedule 3 days in the office and 2 days remote per week.

    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.

    We cant wait to see where this journey takes you!

    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 ().

    Required Experience :

    Intern

    Key Skills

    Accounts Administration,AECOM,Corporate Sales,Documentation,Accident Investigation

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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