Trial Master File & Site Management Intern

GenmabPrinceton, TX
36dHybrid

About The Position

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! 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 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. You'll join a dynamic, global team where you'll collaborate not only with our US colleagues but also with experts from Denmark and the Netherlands—broadening 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.

Requirements

  • Currently pursuing a Bachelor's 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

Nice To Haves

  • 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.

Responsibilities

  • 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 Genmab’s 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.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service