Clinical Drug Supply Manager

Clinical Drug Supply Manager

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Locations: Copenhagen, Princeton, NJ

Time Type: Full time

Posted On: Posted 4 Days Ago

Job Requisition ID: R11309

At Genmab, we’re committed to building extraordinary futures together, by developing antibody products and pioneering 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 searching for an experienced Clinical Drug Supply Manager to be part of Global Clinical Drug Supply Operations in Copenhagen, DK or Princeton, NJ in commuting distance to our office locations to work according to our hybrid work arrangement.

Moving forward with many late-stage trials in the pipeline, the Clinical Drug Supply Manager will be managing outsourcing of packaging, labeling, and distribution of clinical trial supplies for early as well as late-stage Genmab clinical trials. The Clinical Drug Supply Manager will work closely with GMP QA and our CMOs ensuring timely packaging and labeling for our clinical trials as well as IST and PAA for patients with cancer and other serious diseases.

The Clinical Drug Supply Manager must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

The position reports to the Director of Global Clinical Drug Supply Operations based in Copenhagen.

Responsibilities

• Manage and coordinate drug supply and provide IMP for clinical trials, IST, and Pre-Approval Access Programs.
• Manage and coordinate ancillaries, pre-medication, and comparators for clinical trials.
• Set up English Master Label, manage label translation without vendor and approval of label proofs/designs.
• Manage set-up of distribution framework through service providers.
• Define appropriate drug supply activities at CMO necessary for providing drug supplies for clinical trials.
• Contribute to maintenance of SOPs and Work Instructions in the department.
• Perform training of other team members.
• Function as Subject Matter Expert within relevant areas.
• Responsible for being compliant with Genmab’s quality system.

Requirements

• At least 3 years’ experience in handling clinical drug supply, including setting up label text and handling of ancillaries.
• Ability to manage stakeholders internally and externally.
• Experience working with CMO for clinical trial supplies.
• Training in GDP, GMP, and GCP is a requirement.
• Experience working with IST and PAA from a Sponsor perspective will be an advantage.
• Excellent communication skills in English - both oral and written.

Moreover, you meet the following personal requirements:

• You can structure and organize your work.
• You are process-oriented and contribute to continuous improvements.
• You have a quality mindset and can prioritize your work in a fast-paced and changing environment.
• You have good interpersonal and communication skills.
• You can work independently as well as within global teams.
• You are result- and goal-oriented and committed to contributing to the overall success of Genmab.

The Team

You will be part of a highly competent team focused on packaging and labeling of supplies for clinical trials, working closely with the Global Clinical Drug Supply Planning team and our CMOs. Together with the Global Clinical Drug Supply Systems team, the three teams make up the Global Clinical Drug Supply department. We have an international and informal working environment with a high pace while having fun and focusing on one team spirit both within and outside the team and department.

Application

Has this sparked your interest? Then we encourage you to upload your CV and cover letter including your motivation for this position. We screen candidates on a continuous basis and call in for interviews.

Fully remote applicants will not be considered, so please indicate if you are willing to relocate if you are not currently living in commute distance.

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.

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.