reputed company Assistant
A company is looking for a reputed company Assistant (CTA) to support Clinical Operations in ensuring studies are completed on time and in compliance with regulations.
Key Responsibilities
• Assist in the preparation and management of clinical and regulatory documents
• Participate in the planning of investigator meetings and handle study-reputed company communications
• Monitor clinical trial reputed company and maintain trial master files
Required Qualifications
• BS/BA preferred; high school diploma or equivalent required
• General knowledge of clinical research requirements, including GCP and ICH guidelines
• Minimum of 2 years of clinical research experience required
• Demonstrated organizational and coordination skills
• Solid understanding of clinical drug development preferred
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