• Organize and drive execution of key initiatives 
• Assist leaders by creating detailed project plans for tracking critical workstreams, milestones and deliverables
• Standardize communications within the department, providing regular status and progress updates to senior management and core teams
• Strategize with program and senior management for the balancing of competing priorities, challenging timelines, and resource deployment
• Assist with strategic operations, scheduling and throughput planning
• Identify areas for improvement in operations and deploy strategies that drive improvement
• Collaborate closely with the Program Managers to ensure project managers possess accurate information on deliverables and initiatives
• Create dashboards for management review and external partners
• Be a visible proponent of quality culture within Archer
• Provide strategic insight throughout the product development process and ensure strong domain representation in product development and manufacturing services teams
• Support investigations of laboratory and product issues to insure timely, closed loop corrective actions and reports as required
• Track and measuring progress and identify and manage project risk
• Lead execution of ECO/ECR process for assigned projects for ECCB review and approval 

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.
• 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
  • Ability to organize, prioritize, and delegate tasks to efficiently move projects forward.
• For those project managers assigned to Clinical initiatives: 
  • 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

EXPERIENCE:

• 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
• Demonstrated ability to work within a commercial environment and influence with and without authority in a cross functional role
• PMP certification strongly preferred
• Working knowledge of cGMP/CFR/ISO standards & FDA regulations preferred

EDUCATION:   

• Bachelor's degree in a technical discipline

In Colorado, our competitive compensation package includes a base salary starting from $100,000 per year.  In determining the final salary offered, we will evaluate a specific candidate's geographic location, education, skills, and experience.

Invitae offers a competitive total rewards package, which includes healthcare coverage, 401k, and a broad range of other benefits, outlined below:

• Health, dental, vision, short- and long-term disability, and basic life insurance coverage
• Paid time off, holiday pay, parental leave, and other health and wellness supports

At Invitae, we value diversity and provide equal employment opportunities (EEO) to all employees and applicants without regard to race, color, religion, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the San Francisco Fair Chance Ordinance.