The Role & Department As a Senior Associate, Clinical Oversight, you will be in the Clinical Operations team and responsible for independently conducting clinical trial support activities related to assigned trials (including coordination and documentation for CTM; critical documentation including sponsor TMF, record management, trial documentation; etc.). You will report to Director, Head of Clinical Oversight, and work closely with colleagues in Clinical Operations and others. Key responsibilities include:Independently, conduct clinical trial support activities related to assigned trials (including coordination and documentation for CTM; critical documentation including sponsor TMF, record management, trial documentation; etc.) Proactively provide ongoing support to trials in terms of logistics management, sponsor oversight support, and coordination for outsourcing and contract managementProactively provide inputs to CTM & COLT with respect to operations, quality, and compliance within assigned trialsAssist with insurance tracking and coordination as well as budget tool maintenanceAssist in optimization of standardized/pre-described clinical trial coordination processes in assigned areaRequirements – what you must haveBachelor’s or Master’s degree in relevant technical areaThree or more years of direct experience in clinical trial operationsExperience in coordination and support activities for clinical trial conductExperience maintaining and tracking critical documentationWhere you will work This role can be located in Copenhagen, Denmark; Utrecht, the Netherlands; or Princeton, NJ USA and is hybrid or can be remote.For US based candidates, the proposed salary band for this position is as follows:$0.00—$0.00The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as bonuses.About YouYou are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatmentYou bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with diverse backgroundsYou are determined to do and be your best and take pride in enabling the best work of others on the teamYou are not afraid to 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 soLocationsGenmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories. Whether you’re in one of our collaboratively designed office spaces or working remotely, we thrive on connecting with each other to innovate.