Clinical Project Assistant Jobs in Tennessee
Project Assistant Jobs
By RemX | The Workforce Experts
At Knoxville, TN, United States
Clinical Project Associate - Wfh
By Sarah Cannon
At Tennessee, United States
Project Assistant Jobs
By Inceed
At Oak Ridge, TN, United States
Are you looking for an exciting opportunity to join a dynamic clinical research team? We are looking for a Clinical Project Assistant to help manage our clinical trials and ensure that all research activities are conducted in accordance with applicable regulations. This is a great opportunity to gain valuable experience in the clinical research field and make a real impact on patient care.
Overview A Clinical Project Assistant is a professional who provides administrative and operational support to clinical research projects. They are responsible for coordinating and managing the day-to-day activities of clinical research projects, including data collection, data entry, and data analysis. Detailed Job Description Clinical Project Assistants are responsible for providing administrative and operational support to clinical research projects. They coordinate and manage the day-to-day activities of clinical research projects, including data collection, data entry, and data analysis. They also provide support to the project team, including scheduling meetings, preparing documents, and maintaining project records. Clinical Project Assistants may also be responsible for preparing reports and presentations, as well as providing assistance with regulatory compliance. 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 research processes and procedures
• Ability to manage multiple tasks and prioritize workload
• Attention to detail
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical research or related field
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of applicable regulatory requirements
Job Knowledge
• Knowledge of clinical research processes and procedures
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of applicable regulatory requirements
Job Experience
• Previous experience in clinical research or related field
• Experience with data entry and data analysis
• Experience with project management
Job Responsibilities
• Coordinate and manage the day-to-day activities of clinical research projects
• Collect and analyze data
• Prepare reports and presentations
• Maintain project records
• Provide support to the project team
• Assist with regulatory compliance
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