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 & Department
Genmab is now searching for an experienced Senior Clinical Drug Supply Manager to be part of Global Clinical Drug Supply, CMC Operations and work according to Genmab's hybrid work arrangement in Princeton, NJ.
Responsibilities

• Establishes Genmab's global clinical trial supply strategy and oversees execution.
• Advises clinical team on resource constraints and recommends strategies to resolve issues in order to meet key milestones.
• Recommends and implements ways to improve the efficiency of clinical supply processes.
• Ensures systems and tools are in place to support, analyze and optimize global clinical trial supplies e.g. IRT and planning tool.
• Ensures development and management of SOPs, work instructions, processes, systems, and forms governing clinical supplies management in alignment with industry standards and regulatory requirements.
• Serves as the primary point of contact cross-functionally for clinical supplies planning, inventory monitoring, and distribution, etc.
• Ensures compliance with Genmab's quality system.
• Manages team in terms of delivery, goal setting, performance management, counselling, and engagement.
• Manages budget for clinical drug supplies.

Requirements - what you must have

• Bachelor's degree in science or related technical area, or equivalent. Advanced degree/certification preferred.
• 6-8 years of experience in supply chain or related area in pharmaceutical, biotechnology, and/or medical device industry.
• Significant experience in drug supply chain management.
• Significant experience in working with applicable regulatory standards e.g. GMP, GCP, ICH guidelines.
• Experience in managing large/complex projects.
• Demonstrated experience in working with multi-functional and multi-cultural teams.

Where you will work
This role is based in Princeton, NJ USA or Copenhagen, Denmark and requires the ability to commute to and work onsite in the office according to Genmab's hybrid work schedule.
For US based candidates, the proposed salary band for this position is as follows:
$114,375.00---$190,625.00
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

• You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment
• You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with diverse backgrounds
• You are determined to do and be your best and take pride in enabling the best work of others on the team
• You are not afraid to grapple with the unknown and be innovative
• You 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

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.