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Genmab Director, Program Management, Translational & Quantitative Sciences in Princeton, New Jersey

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.

Are you inspired by working in a company with ambitious goals? Our vision is by 2030, Genmab's knock-your-socks-off "KYSO" antibody medicines are transforming the lives of people with cancer and other serious diseases. To support and execute on Genmab's vision, we are looking for an experienced Director, Program Management, Translational & Quantitative Sciences to lead and shape the project management efforts for our Translational & Quantitative Sciences (TQS) department. This TQS PM Lead role reports to the VP, Head of Development Program Management.

The TQS Research PM (RPM) team is accountable for managing cross-functional TQS research activities to support Genmab's products from discovery through clinical development. These activities are primarily driven by scientific leads from Early-/Late-stage Translational Research, Non-Clinical Safety, Diagnostics, Pathology, Translational Medicine Labs, and Data Science and expertise areas. This includes both internally and externally performed research and clinical activities. TQS RPMs ensure effective communication and optimal collaboration in assigned drug development programs, allowing the scientific experts to focus on the science. They create overviews of the required work packages, coordinate TQS scientific governance forums, confirm and inform timeline alignment of both internal and external research activities, and reconcile these to the overall program development timelines.

The TQS PM Lead will manage a team of skilled RPMs to facilitate the project organization for the TQS department. The Directorwill help organize and manage complex projects. They will provide department overarching overviews and information to the TQS Leadership Team. Furthermore, the TQS PM Lead will be a key contributor in optimization of cross-department and cross-functional processes, working to establish increasingly strong connections between various departments and teams across the Genmab sites (NL, US, DK) to align all deliverables.

Success in this role will require developing strong relationships with TQS Functional Leaders and working in partnership with their teams, as well as Discovery PMs and TQS Business Operations Managers. This is a non-laboratory, management position, requiring excellent interpersonal and writing skills, a high level of organization, diplomacy, focus, ability to work under tight deadlines, and strong affinity with biomedical research and knowledge of how Translational Research, Precision Medicine, Pharmacology, and Toxicology impacts drug development.

Responsibilities
Organize, structure, and connect research activities in the Translational & Quantitative Sciences department and ensure alignment with other research departments.
Work with Scientific Project leads and department heads to understand the book of work across the TQS departments.
Collate an inventory of TQS work packages, including timelines and key deliverables. Monitor progress with your team of RPMs, identify opportunities for efficiency or prioritization, and escalate in a timely manner when objectives may be at risk.
Ensure close collaboration with the responsible Scientific Project leads to optimally execute the research activities and facilitate prioritization and decision making.
Support prioritization and timeline alignment between TQS research departments.
Manage cross-functional dependencies and align with internal and external functions for end-to-end integrated project planning.
Help to manage the project information, documentation, and team communications.
Provide overviews of deliverables, timelines, and risks to the TQS Leadership Team.
Create, develop, and iterate formal processes and tools to manage work packages, interdependencies, project resources and budgets, scientific risks, and change management.
Connect key stakeholders and optimize processes to improve effectiveness and ensure program success.
For external research collaborations, support joint research activities in close collaboration with Alliance Management .
Guide scientific project meetings; manage timelines and communication of deliverables towards appropriate governance and scientific forums.
Provide leadership to TQS RPMs. Develop the TQS RPM team, recruit new members and represent TQS RPM in relevant forums.
Within the Portfolio & Project Management department, actively contribute in building program management tools and capabilities.


Requirements

Education:
A minimum of a Bachelor's degree is required
Post-graduate degree in life sciences or engineering is preferred.

Experience:
A minimum of 10 years of experience in biotech/pharmaceutical R&D with at least 5 years in cross-functional program management in translational research or pharmacology.
Proficient in a wide range of project management skills, including maintenance of complex schedules, project budget, change control, cross-team leadership, and risk mitigation.
Strong understanding of how biomarkers, precision medicine, pharmacology, and toxicology impact drug development.
Line management experience, with keen interest in developing people.
Excellent internal/external communication and stakeholder management skills.
An experienced leader who is flexible,...

Equal Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity

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