Clinical Research Associate Jobs in Bismarck, ND
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.
GCP (Good Clinical Practices) and regulatory requirements. + Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality...
Demographic Data for Bismarck, ND
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Bismarck, ND
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Bismarck, ND 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
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Drug Development
- Biology
- Centrifuge
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Written Communication
- Collaboration
- Documentation
- Education Experience
- Bachelor's Degree
- Data Entry
- Reporting
- Microsoft PowerPoint
- 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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