Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity
Core
Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulations.
Role type
Experienced Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Contract Research Organization (CRO)
Required skills
Clinical trial monitoring, regulatory compliance (GCP/SOPs), site qualification, source data verification, adverse event reporting, patient recruitment assessment, risk-based monitoring
Preferred skills
Therapeutic area expertise, international team collaboration, leadership potential
Technologies
CTMS, Microsoft Office
Responsibilities
Conduct on-site and virtual monitoring activities; verify investigator qualifications and resources; review medical records and source documentation; ensure accurate adverse event reporting; assess patient recruitment and retention; complete monitoring reports and follow-up letters.
Seniority
Experienced, hands-on IC
