Clinical Research Associate Jobs in Missouri
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.
Clinical Research Associate II and Senior Clinical Research Associate
- ClinChoice
- MO
- 6 days ago
- MO
- 6 days ago
Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements. Sound knowledge of medical terminology. Fluent in English and local language(s)....
In PersonClinical Research Assistant Opportunities - Multiple Locations Nationwide
- Headlands Research
- Chesterfield, MO
- 30+ days ago
- Chesterfield, MO
- 30+ days ago
supporting clinical trials and working alongside experienced CRCs and investigators Opportunities to learn Good Clinical Practice (GCP), regulatory processes, and study operations Clear pathways for...
In PersonClinical Research Associate, Sponsor Dedicated
- IQVIA Holdings Inc
- Kansas City, MO
- 30+ days ago
- Kansas City, MO
- 30+ days ago
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
In PersonSenior Clinical Research Associate, Early Clinical Development
- IQVIA Holdings Inc
- Kansas City, MO
- 30+ days ago
- Kansas City, MO
- 30+ days ago
Key Responsibilities Conduct all types of site visits-selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines...
In PersonClinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
In PersonSr. CRA 1, Oncology, IQVIA Biotech
- IQVIA Holdings Inc
- Jefferson City, MO
- 60+ days ago
- Jefferson City, MO
- 60+ days ago
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
In PersonIn this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines....
In PersonWhat You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards....
In PersonSenior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading healthcare intelligence and clinical research organization....
In PersonDemographic Data for Missouri
Moving to Missouri? Find some basic demographic data about Missouri below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Missouri
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Missouri offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Fannie Mae
- Good Clinical Practice
- ICH Guidelines
- Study Management
- Sample Preparation
- Institutional Review Board
- Clinical Monitoring
- ICH GCP
- Clinical Trial Management System
- Drug Development
- Biostatistics
- Gene Therapy
- Pharmacovigilance
- Cancer Research
- Biology
- Site Management
- Clinical Trials
- Clinical Operations
- Clinical Research
- Biotechnology
- Neuroscience
- Medical Device Sales
- FDA Regulations
- Oncology
- Data Collection
- Standard Operating Procedures
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Documentation
- Implementation
- Verbal Communication
- Reporting
- Policy Development
- Data Entry
- Collaboration
- Education Experience
- Microsoft PowerPoint
- Bachelor's Degree
- Microsoft Word
- Regulations
- Research Skills
- Microsoft Excel
- Microsoft Office
- Problem Solving
- Staff Supervision
- Scheduling
- Computer Skills
- Time Management
- Leadership
- Communication Skills
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