Clinical Research Associate

Company Description Anova Enterprises, Inc. is a technology enabled CRO that provides a SaaS-based platform, AnovaOS, to streamline access for those involved in research, accelerate throughput of new therapies, and provide a framework for collaboration, quality evidence generation, and scientific insight.
Role Description This is a full-time remote role for a Clinical Research Associate.
The Clinical Research Associate will be responsible for monitoring clinical trials, ensuring compliance with protocols, and overseeing clinical monitoring operations.
The Clinical Research Associate will also be responsible for data collection, analysis, and reporting.
The Clinical Research Associate maintains Trial Master File (eTMF) and is responsible for its accuracy and completeness.
Closely participates in start-up process regarding EC and RA submissions and may assist with ICF creation or update.
Independently performs site evaluation/initiation, training, monitoring, and closure visits and applies risk-based monitoring.
Closely interacts with project team and is responsible for accurate and timely completion of reports, issues/deviation reporting and resolution.
Participates in various work groups and performs other assigned tasks Qualifications Experience in managing and monitoring clinical trials Knowledge of clinical operations and protocols Strong research skills Ability to collect, analyze, and report data Excellent written and verbal communication skills Ability to work independently and remotely Bachelor's degree in a related field, such as life sciences or healthcare Experience with electronic data capture systems is a plus