Associate to Sr. Director, Clinical-Stage Program Management at Kumquat Biosciences Inc

San Diego, California, United States -

Full Time

Start Date

Immediate

Expiry Date

28 Jan, 26

Salary

0.0

Posted On

30 Oct, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Stage Program Management, Project Management, Communication Skills, Leadership, Program Management Tools, GCP Knowledge, GMP Knowledge, GLP Knowledge, ICH Guidelines, Regulatory Pathways, Document Organization, Critical Thinking, Attention to Detail, Collaboration, Strategic Planning, Risk Mitigation

Industry

Biotechnology Research

Description

Description Kumquat Biosciences is committed to the discovery and development of innovative drugs to transform cancer treatments. Kumquat brings together an accomplished management team and distinguished scientific founder to translate innovative research to novel therapeutics. Our team has a proven track record of drug discovery and development, having played pivotal roles in the discovery of multiple clinical-stage compounds as well as approved drug for the treatment of cancer and immune-mediated inflammatory diseases. In this role, you will facilitate the strategic planning, execution, and oversight of multiple clinical-stage programs. You will be responsible for fostering collaborations across internal teams and external partners to advance key milestones and deliverables. The ideal candidate is a servant-minded and inspiring leader with a strong track record and expertise in clinical stage program management and the ability to build lasting working relationships. A passion for accelerating the development of life-changing innovative medicines that offer hope to cancer patients is essential. Job Responsibilities: Facilitate the strategic planning and execution of development milestones for multiple clinical programs. Develop and implement best practices in program management, collaborate with functional leaders to establish integrated program timelines and development plans with clear milestones and deliverables, critical paths and cross-functional dependencies, scenarios analysis and risk mitigation strategies. Facilitate high-impact team meetings with clear agendas, action items, actively monitor program progress to ensure programs on track with attention to detail. Foster strong working relationships with executive and functional leaders and a culture of accountability, collaboration, operational excellence and transparency, data driven and results oriented decision-making process. Drive cross-functional alignment across internal teams with corporate goals and external collaborators. Requirements Below requirements are minimum for associate Director in Clinical Program Management. Bachelor’s degree, advanced degree in life sciences or related field preferred. Minimum 10 years of experience in project management with at least 5 years in clinical stage program management or project leadership roles. Exceptional communication skills and servant-minded leadership. Extensive knowledge of Program Management tools - Office Timeline, Microsoft Project, etc. Work knowledge of GCP, GMP, GLP, ICH guidelines, and regulatory pathways. Excellent document organization and critical thinking skills with attention to details and accuracy. What We Offer Competitive compensation and equity package Comprehensive health and wellness benefits, 401K A mission-driven culture focused on innovation and patient impact

Responsibilities

Facilitate the strategic planning, execution, and oversight of multiple clinical-stage programs. Foster collaborations across internal teams and external partners to advance key milestones and deliverables.