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Fortrea

DCT Lead, Clinical Trial Configuration (Sponsor-Dedicated)

Posted 10 hours ago
5-10 years experience
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AI Summary

Serve as the Clinical Technology SME to lead the implementation and delivery of technology solutions like eCOA and telehealth across global clinical trials. Coordinate effectively with study teams, vendors, and sponsor stakeholders to ensure project milestones, quality standards, and regulatory compliance are met.

Clinical technology. Global studies. Direct sponsor partnership.

We’re looking for an experienced Clinical Technology professional to join a sponsor-dedicated team and lead the implementation and delivery of technology solutions across global clinical trials.

As a Clinical Technology SME, you’ll partner with study teams, vendors, and sponsor stakeholders to help deliver innovative, compliant, and effective technology solutions throughout the clinical trial lifecycle.

What you’ll do

  • Serve as the Clinical Technology SME for assigned clinical studies.
  • Lead study-level implementation of technologies such as eCOA, eConsent, telehealth, medical devices, and COA solutions.
  • Coordinate technology delivery across study teams, vendors, and sponsor stakeholders.
  • Manage priorities, milestones, risks, issues, and escalations to keep technology delivery on track.
  • Apply SDLC principles and support validation, testing, documentation, and inspection readiness.
  • Drive consistent technology standards, quality, and continuous improvement across studies.

What you bring

  • 6+ years of relevant clinical research/drug development experience, including direct clinical technology experience.
  • Hands-on experience implementing, integrating, deploying, or overseeing clinical trial technologies.
  • Strong project management skills and experience working with clinical technology vendors.
  • Knowledge of SDLC, FDA/ICH requirements, GxP, and ALCOA++ principles.
  • Strong problem-solving skills and the ability to manage multiple studies and stakeholders.
  • Bachelor’s degree in Life Sciences, Health Sciences, IT, Computer Science, or a related discipline, or equivalent relevant experience.
  • Fluent English and strong communication skills.

Nice to have

  • Experience in a sponsor-dedicated or FSP model.
  • Experience supporting clinical technology across multiple studies or development programs.
  • Clinical technology validation and testing experience.
  • Experience supporting regulatory audits or inspections.

Ready to bring your clinical technology expertise closer to the sponsor and help shape how technology is delivered across global clinical trials? We’d like to hear from you.

Learn more about our EEO & Accommodations request here.

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