Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. 

 

The Role

 

Genmab is growing and to support this, we are looking for an experienced candidate within Analytics & Visualization.

 

In this role, you will be responsible for growing and maintaining the portfolio of applications and visualizations supporting clinical trial oversight and conduct activities across clinical development functional areas. Facilitation of new requirements and management of daily operations of the business applications in the visualization platform (Qlik Sense). This includes full utilization of your skill set as internal consultant, application developer, and project manager specialized in the various configurations and processes supporting analysis and reporting needs within our clinical trial portfolio.

 

The position is part of a smaller team, and you will have high influence on the global application roll out, set-up and processes and will report to the Analytics & Visualization Lead. You have experience in assessing and implementing ICH GCP requirements into business processes driving sponsor oversight and risk based monitoring activities, helping the team ensure value creation via fit for purpose visualizations and dataflow.

 

You will be subject matter expert in the visualization needs, the underlying business processes the data sources, and relevant integrations with source systems (e.g. EDC, CTMS, ePRO, IRT, CDISC, Safety, QMS, TMF, Project Mgmt., data facilitated by a variety of 3rd parties). You have both experience in Project Management and development/programming experience in visualization tools (preferably Qlik), but not limited to.

 

You are an expert in assessing how to best fulfill business requirements and facilitating data review and analysis via interactive solutions and traditional outputs. You constantly think out of the box and internal customer in mind to ensure solutions are fit for purpose and deliver high business value.

 

Responsibilities

  • Facilitate business requirements, collect needs, assess and propose a way forward, including prototyping and Proof of Concept efforts

  • Manage and lead Application Developer roles and resources within the area of responsibility in the application portfolio, in the development and implementation of standard and customized solutions

  • Data modelling and design of back end (ETL) and front-end (UI) layers

  • Project manage application roll out across trials including planning, development, validation, and implementation activities

  • Engage with super users and maximize use adoption and streamline requirements as well as underlying business processes

  • Design, coordinate, and execute training activities

  • Ensure consistent and quality implementation and use of the visualization platform across trials

  • Keep oversight of end-to-end dataflow, feeding into and reporting out of the applications, incl. oversight and execution of troubleshooting needs and outcomes

  • Ensure applications are kept in validated state. Lead periodic reviews, issue management, patch (risk) assessment, etc.

  • Collaborate with IT to ensure system (IT platform) is kept in a validated state and living to the expectations of the visualization work (upgrades configurations, functionality, add-ons)

  • Optimize development model for application and visualization delivery (stack of SOPs, WIs and associated material)

 

Requirements

  • Extensive experience and in depth understanding of clinical and operational data managed within a clinical trial context, data flow, and clinical data review and reporting requirements

  • Savvy in visualization functionality, best practices, and improvement opportunities

  • Clinical and Operational databases capturing clinical trial data

  • Insights, interfaces, and reports facilitating data review and analysis

  • Understanding of scientifically driven and operationally driven needs

  • Trial planning and conduct processes and steps / levels

  • Visualization and report development and configuration (what can source systems do out of the box, what is best managed by a BI/visualization platform, etc.)

  • Relational data models and programming for visualization and reporting purpose

  • Data interchange and data integrity (standards, methods, technology)

  • CDISC standards

 

Besides all the technical and educational requirements, we need a person with strong communication skills for intense an agile communication with cross functional stakeholders as well as technical experts.

 

You hold a holistic understanding of the overall dataflow, data review and, decision-making outputs in clinical trials and the capability to extend that into complex oncology trials with a variety of data and constant tailoring into new situations and needs. Adaptability for changing needs and handling a series of parallel tasks and discussions.

 

Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.

At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.

 

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.

 

Please note that if you are applying for a position in the Netherlands; Genmab’s policy for all permanently budgeted hires in this location 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.

 

Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with you application on our website https://www.genmab.com/privacy.

 

Scam alert

Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation.  This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.

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ATTENTION: IF YOU WOULD LIKE TO APPLY TO ANY OF OUR AVAILABLE POSITIONS, PLEASE DO SO THROUGH THE LINK IN EACH VACANCY "LINK FOR MORE INFORMATION" "APPLY HERE"! WHO WE ARE Delivering on our promise for patients Founded in 1999 in Copenhagen, Denmark, we are a dual-listed, international biotechnology company specializing in the creation and development of differentiated antibody therapeutics for the treatment of cancer. We are led by an experienced international management team. Our proprietary product pipeline and next-generation antibody technologies are the result of our strong company culture and a deep passion for innovation. We are inspired by nature and the power… Read more