Director, Team Leader, External Data Quality Management, Clinical Data Management job in Princeton
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New Jersey (NJ),
Princeton
Job Code: | R10647 |
Employer: | Genmab |
Category: | Clinical Research |
Location | |
Country: | United States |
State: | New Jersey (NJ) |
City: | Princeton |
Post Date: | 04/25/2024 |
Description | |
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. The Role The Director, Team Leader, External Data Quality Management, Clinical Data Management, at Genmab is operationally responsible for the oversight of External Data Quality Management activities related to effective planning and timely delivery of complete, high-quality, and reliable external data for clinical trials. The Director will provide oversight to ensure end-to-end external data reconciliation/management activities are consistent across the portfolio. The employee will also provide strategic input to support Genmab clinical development programs to ensure external data management excellence. In the role of Team Leader, the employee will be responsible for managing, developing, supervising, and supporting the employees in External Data Management and ensuring that the employees' competencies reflect their responsibilities, as outlined in their job descriptions. The Team Lead will be part of the External Data Management Leadership Team which defines the overall strategy and areas for development of External Data Management. In collaboration with the Senior Director, Team Lead, External Data Management, contributes to and supports the strategic direction of External Data Management functional area and ensures activities and processes support the efficient and effective execution of clinical trials, development of standards, support system oversight activities as well as drive/support audit/inspection readiness activities. Furthermore, it is expected that the employee will lead/support and facilitate process optimizations and process development within External Data Management in alignment with ICH-GCP and relevant guidelines. Responsibilities
Development Operations
Requirements
Where You Will Work
For US based candidates, the proposed salary band for this position is as follows: $0.00---$0.00 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. About You
Locations 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. About Genmab Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies. By 2030, Genmab's 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 locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan. Our commitment to diversity, equity, and inclusion 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 our website . 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 https://www.genmab.com/privacy . 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. |
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