Drimva

Nanopath

Clinical Operations Manager

Cambridge, MA +1 · Manager · Full-time · Posted Mar 12, 2026

Location
Cambridge, MA
Cambridge, Massachusetts, United States
Experience
5+ years in clinical operations, clinical research, or clinical trial management.
Education
Bachelor’s degree in life sciences, nursing, public health, or a related field.

About the job

Leads the planning and execution of Nanopath’s pilot and pivotal multi-site clinical studies supporting FDA clearance.

What you'll do

  • Manage study start-up, site selection, initiation, monitoring, and ongoing study operations.
  • Own IRB submissions, regulatory coordination, and clinical documentation to support GCP compliance.
  • Coordinate sites, reference laboratories, vendors, milestones, risks, and internal study updates.

What they ask for

  • 5+ years of experience in clinical operations, clinical research, or clinical trial management.
  • Experience with study start-up, IRB submissions, and site initiation.
  • Hands-on site-monitoring experience, on-site and/or remote.
  • Understanding of GCP, ICH guidelines, and clinical trial regulations.

Nice to have

  • Advanced degree.
  • Experience building clinical trial infrastructure and teams at early-stage companies.

Model-written summary · the original posting is authoritative

First seen Oct 29, 2026 · Last verified Nov 5, 2026 (UTC)