Clinical Research Associate Jobs in Orem, UT
A Clinical Research Associate (CRA) plays a pivotal role in the biotechnology industry, overseeing various aspects of clinical trials. These include designing, implementing, and monitoring clinical trials, ensuring data integrity, verifying case report forms, providing progress reports, and ensuring compliance with protocols and regulatory requirements. CRAs play a crucial role in the development, testing, and approval of new products in the biotechnology industry by managing the clinical trials that prove their safety and efficacy.
Important skills for a CRA include strong communication and organizational abilities, keen attention to detail, knowledge of clinical practices, and analytical skills. CRAs also need to be proficient in using specialized software for data analysis and trial management. Certifications such as Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP) are typically required. Prior to becoming a CRA, individuals might have roles such as Clinical Research Coordinator, Clinical Trial Assistant, or Research Nurse, gaining necessary experience in managing clinical trials and working in a research setting.
CRA (Community Reinvestment Act) Program Manager
- Sandy, UT (20 miles from Orem, UT)
- 2 days ago
- Sandy, UT (20 miles from Orem, UT)
- 2 days ago
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Demographic Data for Orem, UT
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Orem, UT
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Orem, UT offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Mortgage Lending
- Fannie Mae
- ICH GCP
- Institutional Review Board
- Sample Preparation
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Cancer Research
- Scientific Research
- Drug Development
- Site Management
- Biology
- Physiology
- Clinical Trials
- Neuroscience
- Biotechnology
- Clinical Operations
- Clinical Research
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Phlebotomy
- Affirmative Action
- Collections
- Investigation
- Auditing
- Presentation
- Documentation
- Collaboration
- Data Entry
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Policy Development
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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