PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
As a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will be collaborating with experienced clinical research professionals who are committed to quality, teamwork, and advancing clinical research.
Remote role in Ukraine
Your responsibilities will include:
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
Conduct site monitoring across clinical studies, serving as the link between project teams, sponsors, and sites while protecting data integrity, protocol compliance, and study timelines.
Independently monitor wound care clinical trials, protect data integrity, and ensure protocol and regulatory compliance while coordinating with sites, sponsors, and clinical teams to support quality study delivery.
Manage assigned clinical trial monitoring and site activities, ensuring protocol, regulatory, and ICH GCP compliance while verifying source documents, documenting site findings, and escalating issues.
Manage Brazilian regulatory and ethics submissions across clinical studies, serving as a key contact for authorities and committees while tracking approvals, maintaining documentation, and advising teams on local requirements.
Oversee wound care clinical trials through site monitoring, data quality checks, regulatory compliance, safety reporting, and coordination with sponsors and research teams.
