Clinical Research Associate Jobs in Saint Louis, MO
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.
SUMMARY The Compliance and CRA Officer provides essential management of the banks compliance program. By ensuring this program accurately reflects applicable laws and regulations, developing and...
Demographic Data for Saint Louis, MO
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Saint Louis, MO
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Saint Louis, MO 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
- FHLMC
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Specimen Processing
- Biology
- Drug Development
- Pharmacovigilance
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
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- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
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- Collections
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- Investigation
- Written Communication
- Education Experience
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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