• Develop integrated project management plans and project schedules using progressive elaboration
• Responsible for overall program timelines
• Manage the 'big picture' and help to initiate early on long lead items
• Receive input from subject matter experts and line function project managers
• Provide actionable insights into the Program status, progress, risks, and value
• Facilitate transparency and communication cross-functionally
• Champion best practices to ensure that the scope, business case, objectives and success metrics for projects/Programs/Portfolios are well defined, understood, measured and reported effectively
• Document key decisions and facilitate information transfer both laterally and vertically for the Program
• Facilitate efficient resource allocation within the Program
• Identify and raise project delivery issues and risks for mediation, resolution or escalation to the appropriate level on a timely basis
• Report, share and identify opportunities around Program metrics and KPIs
• Conduct project post-mortems and continuous improvement sessions
• Foster accountability of cross-functional team leads to resolve project issues and ensure project success
• Ensure that cross-functional team leads have a clear understanding of roles and responsibilities for planning and delivering project, goals, deliverables, and issues
• Support the implementation of standard project and business management processes and tools.
• Review, understanding, and compliance with ArcherDX HIPAA Security policies and procedures.
• Safeguarding the privacy and security of protected health information and European Union personal data.
• Processing and handling of European Union personal data only as directed by ArcherDX for purposes of personalized molecular pathology.

EXPERIENCE:

• Must have experience operating at the individual project level for organizational project management.
• Minimum of 5 years' Program/Project Management experience in the diagnostic or pharmaceutical industry.
• Proven ability to coordinate multifaceted projects, including multitasking, deliverables management and timeline management.
• Demonstrate ability to work within a commercial environment and influence with and without authority in a cross functional role.
• Experience in diagnostic development or similar development paradigm

KEY ATTRIBUTES:

• Drive and determination
• Ability to work in a fast paced and dynamic environment
• Understanding of design controls and diagnostic approval process from concept to submission.
• High energy, self-motivated, approachable and articulate team player.
• Demonstrates strong leadership capabilities with the ability to lead a cross-functional team (assay development, laboratory, clinical, software, etc.) through a complex development program.
• Significant experience with clinical trials within a biotechnology, pharmaceutical or biopharmaceutical company.
• Demonstrated ability to design and develop products and to interpret and evaluate clinical data.
• Ability to participate with others as a member of the team to ensure that demanding and difficult projects are handled smoothly and cooperatively to enhance the success of the projects and maintain strong relationships within all parts of the company.
• Strong communication and presentation skills
• Self-starter
• Driven to perform
• Self-directed: needs little explicit direction
• Able to organize, prioritize, and delegate tasks to efficiently move projects forward.

EDUCATION:

• BS/MS/PhD preferred with relevant training in Chemistry, Manufacturing, and/or Biological Sciences or equivalent experience.
• Project management certification (PMP®, PRINCE2®) or equivalent required.