Seagen

Senior Program Manager

Development - Bothell, United States

Description

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to improving the lives of cancer patients goes beyond science, and we believe that every employee has a role in contributing to this mission. By working together with a shared dedication and diverse perspectives, we are able to reach our full potential and make a real difference in the world. Seagen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Put your passion to work at Seagen and join us!

Summary:

Seagen is seeking a highly motivated and experienced individual who will be responsible for supporting cross-functional drug development activities for high priority, early-stage program(s). This position will partner with program and functional leaders and work in close collaboration with the Global Product Team, sub-teams and co-development partners to advance priority programs. The Senior Program Manager will report directly to the Associate Director, Program & Portfolio Management.

Responsibilities:

• Work collaboratively and cross-functionally to coordinate, influence and manage efforts to ensure seamless execution of the global product strategy
• Provide program and project management leadership and support for key functional activities including functional sub-team and working group meeting support, regulatory submission planning and management and/or commercial launch efforts
• Working in coordination with the Program Team Lead, Global Program Manager and functional leads, develop and maintain high-quality, integrated project plans that align with overall program strategy and drive communication, scenario planning and decision making
• Facilitate the identification, management and communication of key program risks and their associated mitigation and contingency plans
• Develop and implement stage appropriate and value-added processes, best practices and tools (integrated timelines, TPPs, stage gate process, governance, core & sub team processes) to increase efficiency and consistency of global product development and team processes/deliverables
• Leverage strong project and organizational knowledge, leadership and facilitation skills to optimize team meetings and facilitate effective governance and decision making
• Build and leverage relationships and networks to improve and enhance team dynamics; proactively identifying opportunities and removing obstacles to drive business results
• Advance program and alliance management best practices and contribute to the operational excellence of Seattle Genetics’ Program Management function with a focus on continuous improvement

Qualifications:

• Minimum of 7 years of multi-disciplinary experience in the pharmaceutical/biotech industry, preferably with experience in global cross-functional drug development
• Late-stage program/project management, regulatory submission planning and/or commercial launch experience highly desirable
• Drug Development knowledge with understanding of other functions relevant to the position which may include: Research, Preclinical, Clinical, Manufacturing, Regulatory and Commercial
• Excellent business acumen, demonstrated ability to align teams to strategy to achieve business and project objectives
• Experience leading and facilitating project team meetings, cross-functional communication and decision making, and ensuring ongoing alignment with internal/external stakeholders
• A proactive and strategic thinker, with strong facilitation, problem-solving and issue resolution skills
• Highly collaborative with outstanding communication and relationship management skills, high emotional intelligence
• Adaptive leadership style with ability to influence teams without formal authority
• Ability to work effectively with cross-functional teams in a highly matrixed global organization
• PMP credential and experience with latest PM tools, software and processes highly valued
• Experience in biologics and oncology, experience working with corporate partners and alliances is desirable

Education:

• Bachelor’s Degree required. Advanced degree (MS, MBA, Ph.D.) in biomedical sciences, business or other disciplines related to drug development highly preferred

As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seagen, please visit www.seagen.com.

Seagen is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law.

The hiring pay range for this position is $131,000 to $169,400 per year based on skills, education and experience relevant to the role. Other components of total compensation include a competitive equity grant at the time of hire (with additional annual grants, and grants upon promotion when applicable), and an annual bonus.

To prevent the spread of COVID-19, and as an integral part of its public health and safety measures, Seagen requires that all newly-hired employees be fully vaccinated against COVID-19 before commencing employment, subject to reasonable accommodation and other requirements of applicable federal, state, and local law.

Apply:

Seagen

Seagen is an Equal Opportunity Employer

Submitted: 12/02/2022