Technical Project Manager

(Project Implementation Team)

VeraSci combines innovative science and technology to advance and improve the clinical trials process for many leading pharmaceutical companies. Our flagship product, Pathway, is a fully customizable Electronic Clinical Outcomes Assessment (eCOA) platform designed to accommodate multiple cognitive, clinical, and functional outcome measures and provides streamlined data collection, improves the quality of test results, and enables seamless and secure data transfer from clinical sites to our cloud-hosted portal.

We are recruiting for a Technical Project Manager who will work with cross functional departments to develop project/program timelines and oversee the operational aspects of technology. Ensure that software product content aligns to support project team requirements, study training, customer acceptance requirements, device preparation, and study delivery schedules.  Monitor and analyze project status to identify potential risks and mitigations, escalate risks to leadership and stakeholders, and follow through to resolution.


  • Develop, communicate, and manage technology deployment plans that include:
    • Study-specific development, validation, and translations
    • Deployment activities: Study setup and configuration; UAT; customer demonstrations; training; device preparation, verification, and shipment
  • Work with assigned project lead, product development, validation, and translations to align technology delivery plan to meet project team and customer study dates
  • Coordinate resources from other teams (Customer Support, Projects) as needed to meet schedule commitments
  • Report study specific needs as requirements in the backlog
  • Work with scientists, business analyst, project team, data management team, and sponsor to ensure product capabilities and study configuration support the study protocol, data collection processes, data review services, export needs, and role-based user experience needs
  • Communicate plans, product dependencies and functional gaps to all stakeholders and escalate risk mitigation actions
  • Demonstrate to customers a solid understanding of product capabilities
  • Document and maintain the release management processes, records, and training plan
  • Other duties as assigned


  • BS/MS degree in Computer Science, Engineering, or equivalent education/experience
  • Experience working with technology platforms in clinical trials preferred (i.e. Site Coordinator, Trial Manager)
  • Experience in managing complex project plans
  • Strong analytical problem solving, negotiating, and communication skills


Qualified candidates should submit a resume and cover letter with salary requirements to:


  • Max. file size: 1 GB.
  • Max. file size: 1 GB.
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