Clinical Research Associate Jobs in District of Columbia
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 - Georgetown University Medical Center Georgetown University
- Washington, DC
- 4 days ago
- Washington, DC
- 4 days ago
Work Interactions The Clinical Research Associate will work directly with the Division Chief, Clinical Trial Principal Investigators, the Clinical Trial Unit research manager, and staff....
Clinical Research Associate - Georgetown University Medical Center
- Washington, DC
- 4 days ago
- Washington, DC
- 4 days ago
Work Interactions The Clinical Research Associate will work directly with the Division Chief, Clinical Trial Principal Investigators, the Clinical Trial Unit research manager, and staff....
Strong knowledge of GCP, ICH guidelines, and regulatory requirements. Experience in site management, patient recruitment, and clinical trial documentation....
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
Req 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....
The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA...
of clinical trials....
Travel Clinical Research Assistant, US Based (Washington, DC)
- Washington, DC
- 90+ days ago
- Washington, DC
- 90+ days ago
Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials....
Demographic Data for District of Columbia
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in District of Columbia
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in District of Columbia offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Federal Housing Administration
- Mortgage Lending
- FHLMC
- 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
- Drug Development
- Site Management
- Physiology
- Clinical Trials
- Biotechnology
- Neuroscience
- Clinical Operations
- Clinical Research
- Anatomy and Physiology
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Affirmative Action
- Collections
- Investigation
- Auditing
- Presentation
- Documentation
- Quality Assurance
- Data Entry
- Collaboration
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Policy Development
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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