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Avania
Posted 47 days agoVerified live 8h ago

Project Manager

Brief overview

Remote
UndergradOr in progress
$130k/yrStated minimum
3+ yrsMinimum
Clinical Trial Project ManagementMedical Device TrialsGlobal Clinical TrialsProject Planning and SchedulingFinancial OversightRisk ManagementMicrosoft OfficeMicrosoft ProjectClinical ResearchClinical OperationsBiostatisticsProgrammingData Management

About the company

Avania is the leading global MedTech-focused CRO, integrating regulatory strategy, clinical development, and market access with confidence.

Job description

Summary

Avania is a clinical research and medical device organization seeking a Project Manager to lead clinical and medical device trials from planning through delivery. The role coordinates cross-functional teams, manages timelines, finances, vendors, risks, resources, and protocol-compliant deliverables while supporting quality and continuous improvement.

Responsibilities

  • Lead US-based and global clinical or medical device trials, coordinating work across Clinical Operations, Biostatistics, Programming, Data Management, and other functions
  • Build and maintain project plans, timelines, milestones, and resource requirements using tools such as Microsoft Project or Gantt charts
  • Monitor project finances, including scope, monthly invoicing, unit- or milestone-based deliverables, revenue performance, profit margins, and potential financial losses
  • Identify when changes in scope or change orders are needed and communicate the supporting rationale clearly
  • Manage external vendors and ensure their work aligns with project requirements, timelines, and quality expectations
  • Review study protocols and ensure deliverables are completed in accordance with protocol requirements
  • Identify risks early, develop mitigation plans, and escalate issues appropriately
  • Maintain regular communication with functional leads to understand priorities, resource needs, dependencies, and progress
  • Navigate competing priorities collaboratively and support effective resource planning across projects
  • Use performance metrics and KPIs to monitor execution and support strategic alignment
  • Contribute to standardized project management processes and a culture of continuous improvement

Skills

  • A college degree
  • Strong project management skills, including timeline development, resource planning, financial oversight, risk management, and execution
  • Clear, confident communication skills and the ability to lead cross-functional teams without needing to be the subject-matter expert in every function
  • The ability to adapt to changing priorities, identify issues early, and maintain focus on quality
  • A collaborative approach and a commitment to empowerment, ownership, and accountability
  • Clinical Operations experience is helpful but not required
  • We also welcome candidates whose clinical research background is in areas such as Biostatistics, Programming, or Data Management and who have developed strong trial leadership skills
  • Ideally 3–5 years of experience in the clinical research industry, including experience leading clinical trials
  • Experience with medical device trials or global clinical trials
  • Proficiency with Microsoft Office applications; experience with Microsoft Project or similar project planning tools is helpful

Qualifications

Must Haves

  • A college degree
  • Strong project management skills, including timeline development, resource planning, financial oversight, risk management, and execution
  • Clear, confident communication skills and the ability to lead cross-functional teams without needing to be the subject-matter expert in every function
  • The ability to adapt to changing priorities, identify issues early, and maintain focus on quality
  • A collaborative approach and a commitment to empowerment, ownership, and accountability
  • Clinical Operations experience is helpful but not required
  • We also welcome candidates whose clinical research background is in areas such as Biostatistics, Programming, or Data Management and who have developed strong trial leadership skills

Nice to Haves

  • Ideally 3–5 years of experience in the clinical research industry, including experience leading clinical trials
  • Experience with medical device trials or global clinical trials
  • Proficiency with Microsoft Office applications; experience with Microsoft Project or similar project planning tools is helpful

Benefits

  • Annual bonus
  • Benefits
  • Remote based role
  • Hands-on coaching and development
  • Opportunities for continued development and career progression

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