Clinical Research Scientist Intern at Genmab

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 TitleClinical Research Scientist InternWhy GenmabOur 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 OverviewThe Clinical Research Scientist (CRS) Intern supports Genmabs drug development efforts by gaining hands-on experience in clinical research science within the Clinical Strategy Team (CST) during a 10-week summer internship. This internship offers exposure to the role of clinical scientist and oncology clinical trials through practical assignments and mentorship. The intern will work closely with other CST members as well as within cross-functional teams contributing to ongoing clinical trial-related activities in order to provide high-quality and timely deliverables.What Youll Do Works in collaboration with other Clinical Research ScientistsAssists in supporting CRS team members in executing the clinical trial in alignment with the clinical development plan (CDP)May assist Sr. level CRS with the development of a trial protocol and to other study-related documentsExposure and education on performing ongoing data review and summarizing efficacy and safety data for interpretation/analysisParticipate in mentorship meetings and contribute to team discussions on process improvements and best practices.Provide general administrative support to the Global CRS team.Assist with the organization and planning of relevant team meetings for the Global CRS Team and CRS leaders including generating agendas meeting logistics developing meeting minutes/action items and archiving.Assist with internal coordination of activities related to the CRS role in support of clinical trials.Provide support with the oversight and maintenance of Global CRS Team folder structure and coordination with relevant stakeholders.Assist with tracking progress across multiple initiatives workstreams and programs including communication to CRS and internal stakeholders as requested.Assist with the management and filing of medical-responsible regulatory documents in the eTMF adhering to required indexing administration with routine review for clinical trial completeness.Provide support for inspection readiness by contributing to the establishment tracking maintenance and quality control of the medical-responsible regulatory documents in the eTMF.Conduct scientific research for publication or indication searches.Create edit and quality check word documents templates PowerPoint presentations and Excel worksheets.Ad-hoc task/projects as assigned.Required Qualifications Capabilities and SkillsCandidate for PhD Pharm D MS or BS degree within the medical biological pharmaceutical science or related disciplineBasic understanding of clinical researchStrong analytical and 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.Genuine interest in clinical research and drug development.Preferred Qualifications Capabilities and SkillsDemonstrates initiative a proactive attitude and eagerness to learn in a fast-paced environment.Effectively communicates and collaborates with team members mentors and stakeholders.Maintains attention to detail and quality in all deliverables while managing multiple tasks.Actively engages with CRS team members while leveraging their feedbackGeneral Intern Information Date/Location/ScheduleInternships will take place June August 2026. This role will be based in Princeton NJ and operate on a required hybrid schedule 3 days in the office and 2 days remote per week.Whats nextHelp 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 YouYou are genuinely passionate about our purposeYou bring precision and excellence to all that you doYou believe in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with a broad spectrum of backgroundsYou take pride in enabling the best work of others on the teamYou can grapple with the unknown and be innovativeYou 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!LocationsGenmab 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 GenmabGenmab 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 Robotics,Machine Learning,Python,AI,C/C++,Data Collection,Research Experience,Signal Processing,Natural Language Processing,Computer Vision,Deep Learning,Tensorflow Employment Type : Full-Time Experience: years Vacancy: 1