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<b>Job title:</b> Programming Manager (Hybrid or Remote)<br />
<br /><b>Company:</b> Genmab</p>
<p><b>Job description</b>: At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.</p>
<p> The Role &; Department:</p>
<p> As a Programming Manager, you will be in the Statistical Programming team and Development Operations organization, responsible for supporting the development of new therapies by performing programming tasks and/or leading a small team to complete various programming efforts within a clinical trial. You will be responsible for ensuring integrity, consistency, and adherence to standards, and ensuring well-structured, high quality data summaries for internal decision making and reporting to health authorities. You will report to the Director, Programming, and work closely with Data Management, Clinical Programming, Statistics, Medical Writing, and other functions as necessary.</p>
<p><b>Key responsibilities include:</b></p>
<ul>
<li>Supports and/or leads programming efforts within a clinical study, depending on background and experience.</li>
<li>As a lead, reviews CRFs for adequacy and consistency.</li>
<li>Supports the establishment and maintenance of Genmab SDTM and ADaM database standards.</li>
<li>As a lead, co-develops analysis related derivation rules, develops data specifications for individual trials and provides guidance to internal programmers or vendors for doing the same.</li>
<li>Performs database consistency checks on databases delivered by vendor.</li>
<li>Performs sponsor oversight of programming activities performed by vendor.</li>
<li>Supports in-house production of tables, figures, and listings by writing programming code following good programming practices.</li>
<li>Supports in-house QC process by applying the appropriate measures (writing of code, review of code/deliverable).</li>
<li>Supports submissions by ensuring programming deliverables are consistent with current agency standards and guidelines.</li>
<li>Supports resource planning and outsourcing of programming activities.</li>
<li>Supports developing and reviewing standard processes and templates.</li>
<li>Supports process improvements within the programming department.</li>
<li>Contributes to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge.</li>
<li>Maintains up-to-date knowledge and competencies within relevant therapeutic and professional areas.</li>
<li>Maintains up-to-date knowledge on relevant regulatory guidelines/requirements.</li>
<li>Proactively develops and maintains good working relationship with stakeholders and colleagues.</li>
<li>Participates and represents programming function in teams and meetings.</li>
<li>Develops, maintains, and ensures proper documentation is available and properly stored (e.g., in eTMF) for programming activities.</li>
<li>Supports development of GenSense Dashboards by providing guidance on data structure, organization, and contents of the Genmab SDTM-databases to the Dashboard- developers and programmers.</li>
</ul>
<p> Requirements &#8211; what you must have </p>
<ul>
<li>Completed Bachelor of Science degree required or equivalent qualifications (e.g., programming experience and skills in the pharmaceutical industry).</li>
<li>At least 3 years of direct experience in programming in the pharmaceutical industry.</li>
<li>Knowledge, experience, and technical proficiency in the SAS software package.</li>
<li>Experience working in a global context.</li>
<li>Proficient in both written and spoken English.</li>
<li>Oncology experience a plus.</li>
<li>Programming in R or Python a plus.</li>
</ul>
<p> As Programmer, it is expected that the employee: </p>
<ul>
<li>Acts as a role model</li>
<li>Proactively engages in department activities</li>
<li>Shares learnings with others</li>
<li>Contributes to various initiatives within the department</li>
<li>Proactively contributes to support a global organization</li>
</ul>
<p> Required competences and skills: </p>
<ul>
<li>SAS programming</li>
<li>Analytical and problem-solving skills</li>
<li>Knowledge of the CDISC, SDTM and ADaM data models: the corresponding structures and organizations of the data</li>
<li>Contextual understanding of the data</li>
<li>Writes efficient, easily maintained and well documented computer programs</li>
<li>Is systematic and organized in writing and archiving computer programs as well as other documentation</li>
<li>Thorough</li>
<li>Proactive, accountable, and goal oriented</li>
<li>Innovative</li>
<li>Team player</li>
<li>Good at sharing knowledge</li>
<li>Takes responsibility and shows initiative</li>
<li>Good communication skills</li>
<li>Good planning and coordination skills</li>
<li>Ability to flexibly work on multiple tasks without compromise of the quality of the work</li>
</ul>
<p><b>Where you will work</b></p>
<p> This role is strongly preferred to be based in Princeton, NJ USA, or Copenhagen, Denmark and is hybrid (according to Genmab&#8217;s onsite and work-from-home flexibility).</p>
<p> Candidates who must be remote (not within commuting distance to Genmab offices) could be considered.</p>
<p> For US based candidates, the proposed salary band for this position is as follows:</p>
<p> $95,625.00&#8212;$159,375.00</p>
<p> The 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.</p>
<p><b>About You</b></p>
<ul>
<li>You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment</li>
<li>You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving</li>
<li>You are a generous collaborator who can work in teams with diverse backgrounds</li>
<li>You are determined to do and be your best and take pride in enabling the best work of others on the team</li>
<li>You are not afraid to grapple with the unknown and be innovative</li>
<li>You have experience working in a fast-growing, dynamic company (or a strong desire to)</li>
<li>You work hard and are not afraid to have a little fun while you do so</li>
</ul>
<p><b>Locations</b></p>
<p> Genmab 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.</p>
<p> About Genmab</p>
<p> Founded in 1999 in Copenhagen, Denmark, Genmab is an innovative biotech company that has become a leader in antibody biology and innovation. Our product pipeline and next-generation antibody technologies are the result of our strong company culture, a deep passion for innovation, and desire to transform cancer treatment and serious diseases.</p>
<p> When you work with us, you’ll be part of a warm, fun, dynamic community, and team up with some of the best, most authentic individuals in locations around the world, who care deeply and share in a relentless drive to innovate and create transformational medicines. People who are candid, impact-driven, and a little unconventional; who seek out and embrace the opportunity to build new and bold futures within a rapidly growing and innovative biotech company; who bring their full selves to work and show up for each other &#8211; rolling up their sleeves to get the job done. This translates into a place where you can be authentically you; are empowered to innovate, build solutions, and execute; feel cared for and supported in growth; and are a critical part of changing the lives of patients around the world through transformative cancer treatment.</p>
<p> Our commitment to diversity, equity, and inclusion</p>
<p> We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information. Learn more about our commitments on .</p>
<p> 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 .</p>
<p> Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.<br />
<br /><b>Expected salary</b>:<br />
<br /><b>Location</b>: Princeton, NJ<br />
<br /><b>Job date</b>: Wed, 03 Jan 2024 06:47:15 GMT</p>
<p><a href="https://jobviewtrack.com/en-us/job-4c1d417f4809001a42546d02060009021722241a0614584a5040440a084e6a154e020f041c6528411a090e1658296f48400b1b0b2524520c0f130f0a08491a0f68421f1c081a/f18d810446a7d9fd1cb0ec3fbf51f150.html?affid=d54dda8fa2db24c8445c282b3d357966"><b>Apply for the job now!</b></a></p>
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