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Clinical Trial Assistant Jobs in California

Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Assistant-1 Jobs
By Cue Health At San Diego, CA, United States
Effective organizational and time management skills; ability to manage multiple assignments and changing priorities
Demonstrate commitment to the implementation and effectiveness of Cue’s Quality Management System
Knowledge of applicable clinical research regulatory requirements (e.g., GCP and ICH GCP)
Create, manage, and audit clinical trial master files and investigator site binders
A minimum of 1 year of experience in clinical research or related field
Previous experience in creating, managing, and auditing clinical trial master files and investigator site binders
Clinical Trial Assistant Jobs
By Corcept Therapeutics At Menlo Park, CA, United States
Assist project team with study specific documentation including filing to the Clinical Trial Management System and Trial Master File
Preferred Skills, Qualifications and Technical Proficiencies:
Track clinical supply inventory at sites and manage the site drug re-supply process
Set-up and maintain tracking system with oversight of manager
Develop working knowledge of company standard operating procedures (SOPs) and FDA regulations related to clinical studies
Familiarity with applicable regulatory requirements, Good Clinical Practice/ICH and Good Documentation Practices
Clinical Trial Assistant (Cta)
By Cytokinetics At , South San Francisco, 94080, Ca $31.50 - $38.50 an hour
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant (Cta)
By Cytokinetics At South San Francisco, CA, United States
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant Jobs
By Abbott Laboratories At , San Diego, Ca $24 - $49 an hour
To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
To provide general administrative support to the Clinical Affairs Department and assistance to department Manager(s) and Director(s).
Research or health care related academic or work experience preferable.
Good written and verbal communication skills.
To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.

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