From drug development to improving quality of life, clinical trials professionals are essential. IDDCR Global Consulting connects top talent with leading life sciences companies across oncology, cardiology, respiratory, and neurological research.
CRAs ensure clinical trials are conducted according to the study protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
Clinical Research Coordinator (CRC)
Works at the study site (e.g., hospital, clinic) and is responsible for the day-to-day conduct of the trial. They screen patients, collect data, and maintain study records.
Clinical Trial Assistant (CTA)
Provides administrative support to the clinical research team, including CRAs and CRCs. They may assist with regulatory documents, tracking study supplies, and scheduling site visits.
Medical Monitor
A physician who provides medical oversight for the trial, ensuring patient safety and data integrity.
