Clinical Trial Assistant - Oncology - Palo Alto, Ca
By ICON At , San Jose
Support clinical trial registration and disclosure on websites per applicable regulatory requirements
At least 1 year experience as a CTA, CRC, or other role in clinical trials.
Proven organizational and presentation skills
Ability to manage multiple tasks with meticulous attention to detail
Excellent written and verbal communication skills
Good knowledge of the ICH/GCP

Are you looking for a rewarding career in clinical research? We are looking for a Clinical Trial Assistant to join our team and help us make a difference in the lives of patients. As a Clinical Trial Assistant, you will be responsible for coordinating and managing clinical trial activities, ensuring compliance with regulatory requirements, and providing administrative support. If you are passionate about clinical research and have excellent organizational and communication skills, this could be the perfect job for you!

Overview A Clinical Trial Assistant (CTA) is a professional who assists in the management of clinical trials. The CTA is responsible for providing administrative and operational support to the clinical trial team. This includes tasks such as data entry, tracking and filing documents, and coordinating with other departments. Detailed Job Description A Clinical Trial Assistant is responsible for providing administrative and operational support to the clinical trial team. This includes tasks such as data entry, tracking and filing documents, scheduling meetings, and coordinating with other departments. The CTA is also responsible for ensuring that all clinical trial documents are accurate and up-to-date. The CTA may also be responsible for preparing reports, tracking progress, and providing feedback to the clinical trial team. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite
• Knowledge of clinical trial processes and regulations
• Attention to detail
• Ability to multitask
• Ability to work under pressure
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical trials or research
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
Job Knowledge
• Knowledge of clinical trial processes and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of data management systems
Job Experience
• Previous experience in clinical trials or research
• Experience in data entry and data management
• Experience in preparing reports and tracking progress
Job Responsibilities
• Data entry and data management
• Tracking and filing documents
• Scheduling meetings
• Coordinating with other departments
• Preparing reports and tracking progress
• Ensuring accuracy and up-to-date clinical trial documents
• Providing feedback to the clinical trial team