Global Project Manager - Personalized Healthcare jobs in United States
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Nesco Resource · 1 day ago

Global Project Manager - Personalized Healthcare

Nesco Resource is a company focused on personalized healthcare, seeking a Global Project Manager to oversee various project management aspects from concept to completion. The role involves developing detailed work plans, managing resources and budgets, and ensuring quality implementation in projects related to Companion Diagnostics product development.

ConsultingHuman ResourcesStaffing Agency

Responsibilities

Drives the project/product from the original concept through completion by developing and directing detailed work plans, schedules, project estimates, spending, resource plans, and status reports
Own project/program/product structures for Companion Diagnostics (CDx) product development & product care activities including communication management, timelines, resource and budget plans, progress and cost control, and risk management
Create, coordinate, and maintain integrated project plans including dependencies, resources and budgets, allowing the teams to work efficiently and effectively
Accountable for quality implementation in projects in the following areas: Project risk management; Critical path analysis; Scenario creation and analysis; Budget; Robust planning
Proactively own and drive integrated project plans including dependencies, resources and budgets allowing the teams to work efficiently and effectively
Execute project management processes including guiding and managing preparation for milestone reviews, capacity reviews (cQCR, SCR & fQCR), etc., as applicable & may lead improvement initiatives
Follow best practices in project/product teams and foster continuous improvement by sharing best practices and knowledge among peers
Select project methodology and apply agile methods as appropriate, including coaching and guiding teams in project methodology, including agile practices (with Project/Program Leads or PMC management if appropriate)
Establish, measure, and report the Key Performance Indicators (KPIs), standard metrics, Objectives and Key Results (OKRs) or Outcome Based Planning (OBPs) key results for projects enabling teams and functions to measure and improve quality, efficiency and effectiveness
Act as a trusted advisor with a 360° view on all levels to advise and support the project/product teams as well as the broader organization in the holistic planning; project risk management; scenario creation as well as critical path analysis with the aim to ensure an optimized value delivery
Serve as a single point of contact & control for project and program data collected from the functions
Lead project team meetings and foster knowledge sharing between project/product teams and sub-chapters to enhance project effectiveness and optimized delivery
Identify project risks and describe potential implications for budget, timeline and scope
Identify gaps, potential bottlenecks or delays, challenge assumptions and propose options to close gaps and get projects back on track while communicating issues proactively to stakeholders
Manage project/product team information to support the teams themselves, the Life Cycle Teams (LCTs) and/or other governing body decision making
Frequently provides high level/pre-defined and recent planning data for scenario analysis and decision making on a portfolio level
Serve as an Agile Program Manager as defined by Scaled Agile Framework (SAFe) where applicable
Other duties as assigned by leadership

Qualification

Agile MethodologiesRisk ManagementProject ManagementClinical Biomarker DevelopmentRegulatory SubmissionsBudget ManagementCommunication ManagementContinuous ImprovementScenario AnalysisTeam Leadership

Required

You hold a Bachelor's degree, preferably in a Life Sciences field
You have 4 years of experience in project management / engineering/ business in the diagnostic, medical device, pharmaceutical or biotech industry leading product development and product care projects
You have at least one year of experience in the following areas: clinical biomarker or In Vitro Diagnostic development, companion diagnostic development, analytical and clinical validations, regulatory submissions, instrument/systems development, or program management
You have one year of experience in a regulated industry (e.g. FDA 21 CFR part 820, ISO 13485, ISO 9001)

Preferred

You hold a Master's degree, preferably in a Life Sciences field, and 6 years project management / engineering/ business experience in the diagnostic, medical device, pharmaceutical or biotech industry leading product development and product care projects
Alternatively, you hold a Ph.D with 3 years project management experience in those areas
Prior 3 years in clinical biomarker or In Vitro Diagnostic development experience in companion diagnostic development, analytical and clinical validations and regulatory submissions or instrument development and program management

Benefits

MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Company

Nesco Resource

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Nesco Resource s an Staffing and Recruiting firm.

Funding

Current Stage
Late Stage

Leadership Team

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Michael McDonald
Executive Vice President of Finance and Chief Accounting Officer
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