Systimmune

The Sr. CRA manages and oversees clinical study sites to ensure data quality and patient safety in compliance with ICH-GCP guidelines. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.

The Sr. CRA is responsible for managing and overseeing clinical study sites to ensure data quality and patient safety according to ICH-GCP guidelines. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.

The medical writer manages and oversees the production of high-quality clinical documentation, including protocols, reports, and regulatory briefing materials. They ensure all documents meet scientific accuracy, regulatory guidelines, and established templates for submission to authorities.

The Senior CRA Contractor manages clinical study sites to ensure patient safety, protocol compliance, and data integrity. Responsibilities include conducting various site visits, monitoring enrollment, and collaborating with CROs and internal stakeholders.

The CRA II manages and oversees clinical study sites to ensure data quality and patient safety in compliance with ICH-GCP and local regulations. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.