Castor

Delightful for patients, effortless for study teams, risk-free for sponsors.

Principle Project Lead

Full TimeRemoteTeam 201-500H1B No SponsorCompany SiteLinkedIn

Location

United States + 43 moreAll locations: United States, Canada, United Kingdom, Germany, France, Estonia, Portugal, Hungary, Poland, Ukraine, Romania, Bulgaria, Czech Republic, Slovakia, Belarus, Moldova, Republic Of, Sweden, Greece, Belgium, Italy, Ireland, Switzerland, Netherlands, Finland, Malta, Denmark, Lithuania, Croatia, Spain, Austria, Bosnia And Herzegovina, Iceland, Luxembourg, Macedonia, The Former Yugoslav Republic Of, Montenegro, Norway, Serbia, Slovenia, Albania, Cyprus, Latvia, Monaco

Posted

1 day ago

Salary

Not specified

No structured requirement data.

Job Description

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more.

Role Description

As a Principal Project Lead, you will lead our most complex, multi-component, multi-country studies, serving as a subject matter expert. Your value to the business lies in your critical thinking and ability to translate high-level, often vague requirements into robust, technically and operationally sound project architectures.

  • Navigate increased variables and technical and operational dependencies that come with complex studies.
  • Operate with minimal oversight, acting as the pivotal bridge and consultant to the customer.
  • Take ownership of the end-to-end delivery from ensuring internal project cohesion to leveraging your risk expertise.
  • Confidently articulate challenges and guide external stakeholders to the best possible solution.

Qualifications

  • Proven expertise in managing highly complex projects within the Software Development Lifecycle (SDLC) for clinical software.
  • Strong understanding of EDC/CDMS, eConsent and eCOA solutions, services and operational strategies.
  • Experience with eCOA services scale licensing, translations, device provisioning, Helpdesk and data management.
  • Strong experience of using project tools such as Jira, Confluence and Microsoft Project (or equivalent).
  • Deep understanding of the regulatory landscape and industry trends to guide project strategy.
  • Comprehensive knowledge of clinical study operations, ensuring technical solutions align with site workflows, patient centricity, and study-specific operational requirements.
  • Direct experience or foundational understanding of Real-World Evidence (RWE) studies, including the unique data capture and longitudinal tracking needs of late-phase research.
  • Self-starter who masters the art of remote collaboration.
  • Ability to give and receive direct, data-driven feedback necessary to win as a team.

Requirements

  • Accepting candidates +2/-2 CET. At this time, we cannot accept applications from France, Germany, Spain, Bulgaria, or Switzerland.

Benefits

  • Unlimited annual leave with a 25-day minimum. We don’t just allow time off; we expect you to take it.
  • Once a quarter, the whole company shifts gears for downtime weeks—no new shipping, just a week for deep focus, learning, or catching up.
  • AI-first culture with tools and training to ensure you’re spending your energy on high-value work, not manual repetition.
  • All team members are offered options through our Employee Stock Option Plan (ESOP).
  • Free access to Open Up for mental health, specialized sleep courses, and a budget for your home office.
  • A guaranteed "Happy Holidays" bonus every December.

Company Description

At Castor, we’re modernizing the backbone of clinical research. We provide a modular cloud platform designed to run trials end-to-end, with a robust Electronic Data Capture (EDC) system, eConsent for recruitment and screening, and eCOA to accurately capture patient-reported outcomes.

We are a remote-first company built on the belief that talented people do their best work when they have the agency to manage their own lives.

Job Requirements

  • Proven expertise in managing highly complex projects within the Software Development Lifecycle (SDLC) for clinical software.
  • Strong understanding of EDC/CDMS, eConsent and eCOA solutions, services and operational strategies.
  • Experience with eCOA services scale licensing, translations, device provisioning, Helpdesk and data management.
  • Strong experience of using project tools such as Jira, Confluence and Microsoft Project (or equivalent).
  • Deep understanding of the regulatory landscape and industry trends to guide project strategy.
  • Comprehensive knowledge of clinical study operations, ensuring technical solutions align with site workflows, patient centricity, and study-specific operational requirements.
  • Direct experience or foundational understanding of Real-World Evidence (RWE) studies, including the unique data capture and longitudinal tracking needs of late-phase research.
  • Self-starter who masters the art of remote collaboration.
  • Ability to give and receive direct, data-driven feedback necessary to win as a team.
  • Accepting candidates +2/-2 CET. At this time, we cannot accept applications from France, Germany, Spain, Bulgaria, or Switzerland.

Benefits

  • Unlimited annual leave with a 25-day minimum. We don’t just allow time off; we expect you to take it.
  • Once a quarter, the whole company shifts gears for downtime weeks—no new shipping, just a week for deep focus, learning, or catching up.
  • AI-first culture with tools and training to ensure you’re spending your energy on high-value work, not manual repetition.
  • All team members are offered options through our Employee Stock Option Plan (ESOP).
  • Free access to Open Up for mental health, specialized sleep courses, and a budget for your home office.
  • A guaranteed "Happy Holidays" bonus every December.

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