Technical Project Manager

NeoGenomics Laboratories

8d•Remote

About The Position

As a Technical Project Manager you will serve as a strategic leader and subject matter expert in research and development to drive the successful outcomes of key programs and initiatives. You will provide expert guidance and strategic counsel to shape the direction of critical programs, aligned to organizational goals. This role will involve overseeing budgets, monitoring program performance and mentoring cross functional team members.

Requirements

Bachelor’s Degree required, advanced degree (MS, PhD) in life sciences, engineering, or related field preferred
12+ years’ project management experience preferably in Medical Device or IVD Global industry, specifically engaged in product development systems, logistics and deployment of products with commercial role out experience
Experience working in cross-functional teams, especially with software engineers, bioinformaticians and wet lab scientists
Experience managing molecular diagnostic assay / genetic test development and validation projects under design control and in compliance with CAP/CLIA and/or FDA regulations
Expertise as an alliance and/or collaboration manager is preferred
Knowledge of clinical diagnostics

Responsibilities

Develop and implement high level program strategies and work plans to influence and achieve program goals
Serve as strategic advisor to the Core Leadership team, acting as a spokesperson for cross functional alignment and key product deliverables
Provide leadership and oversight ensuring successful completion of projects including resource allocation and monitoring
Own overall responsibility and accountability for Program Plan from the planning phase through delivery
Manage and implement change effectively
Lead collaboration between cross-functional teams, with software engineering, bioinformaticians and wet lab scientists
Track and report on project metrics to show progress of deliverables to plan
Provide decision and administrative guidance as required for project sponsors, decision makers, and stakeholders involved in the project, project and portfolio
Create a culture of compliance and quality excellence across process workflow, particularly in new assay formats under design control standards
Manage molecular diagnostic assay / genetic test development and validation projects under design control and in compliance with CAP/CLIA and/or FDA regulations
Lead evaluation and communication of program/project risks, recommending proactive mitigation strategies
Maintain relationships and alignment with internal and external partners
Map out program and/or project framework and build estimated timeline for work to enable efficient and transparent execution.
Establish solid relationships and elicit agreement from a variety of stakeholders