Remote (Country)

Natera is hiring a Manager, Clinical Project Management

About the Role

Natera is hiring a Manager, Clinical Project Management to drive continuous process improvement and establish best practices for data operations workflows. You will oversee all end-to-end clinical trial and patient matching operations, serving as the critical liaison between trial sites, sponsors, principal investigators, and Natera.

What You'll Do

  • Account for the execution and timelines of patient matching and clinical trial support activities, optimizing speed, quality, and cost.
  • Support business development by participating in bid defenses and leading presentations for regional studies.
  • Serve as a change advocate and the primary liaison for sponsors, investigators, and vendors, resolving concerns and queries.
  • Proactively identify project risks and develop mitigation strategies to ensure milestones are met on time and within budget.
  • Implement and maintain quality control processes to ensure data integrity and adherence to protocol and regulatory guidelines.
  • Develop comprehensive project plans, SOPs, timelines, budget estimates, resource allocation, and risk management strategies.
  • Set objectives for project teams, communicate effectively, and assess performance.
  • Oversee the creation and maintenance of accurate trial master files (TMF), study binders, and all other site and trial forms.
  • Exhibit deep familiarity with protocols, ensuring all procedures are followed.
  • Lead engagement with providers to facilitate patient screening, recruitment, education, and eligibility discussions.
  • Lead cross-functional engagement with software engineers, data specialists, IT, and product management to deploy virtual trial site activity and maintain EDC systems.
  • Arrange and lead sponsor and project meetings, provide executive reporting, and track KPIs.
  • Maintain relevant clinical or technical licensures and attend conferences.
  • Mentor and train junior project staff and contribute to process improvement.
  • Support staff recruitment and onboarding.

What We're Looking For

  • 5-6 years of experience providing project or program management leadership for projects handling clinical data or research.
  • 4-5 years experience hosting and leading meetings, standup ceremonies, and coordinating project timelines.
  • 3-4 years of experience supporting cancer clinical trials.
  • Direct experience managing study binders, trial master files, supporting study start-up and close, tracking metrics, and identifying and enrolling study subjects.
  • Demonstrated commitment to data integrity, quality control, and adherence to HIPAA and data privacy regulations.
  • Proficient with Microsoft Office Suite or Google Suite, including creating pivot tables, generating reports, data analysis, and using clinical data systems.
  • Must hold an active PMP or relevant project management certification.
  • Deep knowledge of and experience working in remote and decentralized clinical trials.
  • Excellent written and verbal communication skills, with the ability to collaborate with PIs, sponsors, patients, and non-clinical teams.
  • Proven ability to work independently, manage time effectively, prioritize tasks, and meet strict deadlines.
  • A high level of initiative, self-motivation, and in-depth attention to detail.
  • Capable of working as part of a team on high-visibility projects with high rates of communication.
  • Ability to respond to shifting priorities and changes.

Nice to Have

  • U.S. licensed Nurse, PA-C, NP, or DNP with a Master’s degree in health sciences.
  • Strong understanding of medical terminology, disease processes (especially cancer), clinical data, and genetic testing.
  • CCRC or CRA certification.

Technical Stack

  • Microsoft Office Suite
  • Google Suite
  • Clinical data systems or databases
  • Electronic data capture (EDC) systems

Benefits & Compensation

  • Compensation: $119,000 - $148,700 USD
  • Comprehensive medical, dental, vision, life and disability plans
  • Free testing for employees and their immediate families
  • Fertility care benefits
  • Pregnancy and baby bonding leave
  • 401k benefits
  • Commuter benefits
  • Generous employee referral program

Work Mode

This is a remote position open to candidates anywhere in the United States.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment and welcome people of different backgrounds, experiences, abilities and perspectives.

Required Skills
Microsoft Office SuiteGoogle SuiteClinical Data SystemsElectronic Data Capture (EDC) SystemsProject ManagementClinical ResearchCross-functional Team LeadershipBudget ManagementVendor ManagementRegulatory ComplianceICH-GCP GuidelinesStakeholder CommunicationProcess Improvement
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About company
Natera

A global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. A rapidly-growing diagnostics company with proprietary bioinformatics and molecular technology for analyzing DNA.

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Job Details
Category management
Posted 2 months ago