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Senior Project Manager, Global Clinical Supply Chain Strategist
2 months ago
We are seeking an experienced Senior Project Manager, Global Clinical Supply Chain Strategist to join our team at Genmab. As a key member of our Global Clinical Drug Supply Planning, Operations & Systems team, you will play a critical role in leading and supporting the development and implementation of global clinical supply chain strategies and operations.
Key Responsibilities- Develop and maintain integrated project plans and technical blueprints that consolidate project schedules, resources, and budgets.
- Monitor and control project integration to ensure successful project execution and delivery.
- Facilitate effective communication and collaboration between cross-functional stakeholders and project teams to ensure project alignment and integration.
- Identify and manage project dependencies and potential conflicts to ensure seamless project execution.
- Develop and maintain global processes for Global Drug Clinical Supply Strategy & Integration.
- Collaborate with stakeholders to ensure process and procedures flows are maintained for the clinical supply stakeholders, cross-functional team, and regional teams.
- Lead the development and implementation of process improvements and digital solutions.
- Ensure process optimization, compliance, and sustainability.
- Provide training, guidance, and support for process improvements and other continuous improvement efforts.
- Align, continuously, processes with evolving business requirements, goals, and strategic changes, while providing inputs to risk management.
- Develop innovation goals, prioritization, and operational/projects plans for global clinical drug supplies in partnership with R&D Teams and enabling functions.
- Optimize end-to-end supply operations across therapeutic areas and remove bottlenecks.
- Track and forecast resource capacity, utilization, and allocation in collaboration with global clinical drug supply.
- Establish and maintain financial transparency for all projects, trials, and initiatives, while identifying ways to reduce cost and overall waste of supplies and resources.
- Track key performance indicators (KPIs) to measure performance and implement corrective and preventative actions.
- Monitor and manage the performance of external service providers.
- Assess and mitigate operational risks and ensure compliance with regulations and internal processes.
- Identify areas for improvement and implement changes to enhance efficiency, productivity, and quality.
- Foster a culture of continuous improvement and innovation.
- Maintain a deep understanding of continuous improvement, development strategy, risk management, and industry trends to drive informed decision-making.
- Language ability – Advanced Proficiency in speaking and writing in Chinese (Simplified).
- Minimum of a completed Master's degree with +8 years of experience, or completed PhD degree with +6 year of experience.
- Experience in handling integration management, process and continuous improvement management, digital or data technology, operations, supply chain, manufacturing, ERP, clinical supply chain, logistics, preferably in the pharmaceutical or biopharmaceutical industry.
- Broad and Diverse experience in working with trial management for global clinical drug supply and supply functions.
- Knowledge and understanding of GMP, GDP, and GCP. Supply Chain systems and processes.
- Strong desire to exploit emerging technologies for better business outcomes.
- Proven experience working in teams.
- Ability to work successfully under pressure in a fast-paced environment and with tight timelines.
- Ability to be proactive, enthusiastic, and goal orientated.
- A team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders to support the execution of tasks.
- Strong communication skills in English - both oral and written.
- Ability to travel to China periodically if necessary (preferred but not required).
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 (KYSOTM) 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.
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.
