Clinical Research Associate

About the role
Dasher Neuroscience is hiring a full-time, US-based Clinical Research Associate to serve as our sponsor-side monitor for US clinical trial sites. This is a remote role with regular travel to sites across the United States; candidates located near a major airline hub are preferred.
Responsibilities
Conduct site qualification, initiation, interim monitoring, and close-out visits per the monitoring plan
Perform source data verification and review; ensure compliance with the protocol, ICH-GCP, and applicable FDA regulations
Manage assigned sites: build investigator and site staff relationships, resolve data queries and protocol deviations, and track corrective actions
Verify investigational product accountability and essential document completeness at sites
Maintain CTMS records, write trip reports, and follow up on action items within required timelines
Collaborate with the CRO team, data management, and internal clinical operations
Qualifications
5–12 years of clinical monitoring experience as a CRA, Senior CRA, CRA II/III, Lead CRA, Clinical Trial Monitor, or Clinical Monitor at a sponsor or CRO; sponsor-side experience strongly preferred
Strong working knowledge of ICH-GCP, clinical monitoring, site management, CTMS, and EDC systems
Bachelor's degree in life sciences or nursing (BSN); prior study coordinator or research nurse experience is welcome
CCRA (ACRP) or CCRP (SOCRA) certification preferred
Strong communication, organization, and documentation skills
Authorized to work in the United States; able to travel regularly

Work arrangement
Yes