Lead Site Clinical Research Coordinator

Salma Health · Fremont

Posted
19 days ago
Last confirmed live
1 day ago

What this role involves

The Lead Site Clinical Research Coordinator will establish research operations at Salma Health's Fremont clinic, managing day-to-day study conduct for the ATLAS study and sponsored trials. Responsibilities include study management, participant coordination, data management, regulatory compliance, and collaboration with sponsors and IRB. The role requires a Bachelor's degree and at least 3 years of clinical research experience, with strong regulatory background.

Skills this posting asks for

  • clinical research
  • gcp
  • ich-gcp
  • fda regulations
  • irb submissions
  • regulatory submissions
  • electronic data capture
  • redcap
  • medidata rave
  • informed consent
  • phlebotomy
  • ecg
  • vital signs
  • data management
  • source document verification
  • sponsor monitoring
  • audits
  • citi program
  • protocol development
  • adverse event reporting

Requirements

  • 3 years of experience
  • Level: lead
  • Remote policy: onsite

From the employer’s posting

The Lead Site Clinical Research Coordinator (CRC) is the founding coordinator for Salma Health's Fremont clinic, responsible for establishing research operations at the site and managing day-to-day study conduct, including the ATLAS study and sponsored trials. The role reports directly to the VP of…

Read the full description on Salma Health’s careers page

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