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Clinical Trial Assistant Jobs in Arkansas

Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Assistant / Trial Documentation (Tmf)
By Apex Systems At United States
1. Provide start-up and ongoing trial regulatory document management
5. Setup and manage regulatory document trackers/reports as assigned.
6. Maintain a professional approach respecting the dignity and confidentiality of associates, manager, and vendors.
11. Maintain CEUs for SOCRA or ACRP certification.
• Oncology experience preferred. Prior experience managing flow of clinical trial regulatory documents preferred
4. Ensure quality product deliverables at all times.
Clinical Trial Lead Jobs
By Avania At United States
Ability to work concurrently on multiple protocols and procedures; organizational, time management skills and problem-solving abilities
RN or BA/BS degree in a science/life science, engineering or health-related field plus a minimum 4 years monitoring experience
Experience as mentor and trainer for new CRAs
Excellent communication skills; demonstrated professional writing proficiency
Experience generating project-specific training presentations and coordinating necessary training
Ability to generate monitoring tools; experience generating and giving professional presentations

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