Clinical Research Associate Jobs
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.
Principal Associate, CRA Strategy & Program Management - Data Management Team
- Richmond, VA
- 29 days ago
- Richmond, VA
- 29 days ago
Principal Associate, CRA Strategy & Program Management - Data Management Team Within Capital One, External Affairs (EA) is an organization dedicated to delivering on Capital Ones Mission by...
Knowledge of the International Conference on Harmonization (ICH) guidelines for Good Clinical Practice (GCP) Current CITI certification in Human Subjects Research and Good Clinical Practice, highly...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I - Biomedical Imaging Research Institute
- Beverly Hills, CA
- 10 hours ago
- Beverly Hills, CA
- 10 hours ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I - Heart Institute
- Los Angeles, CA
- 30+ days ago
- Los Angeles, CA
- 30+ days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I, PER_DIEM -Heart Institute
- Los Angeles, CA
- 10 hours ago
- Los Angeles, CA
- 10 hours ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I - Karsh Division of Gastroenterology and Hepatology (Per Diem)
- Los Angeles, CA
- 30+ days ago
- Los Angeles, CA
- 30+ days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I (Per Diem) - Smidt Heart Institute
- Los Angeles, CA
- 30+ days ago
- Los Angeles, CA
- 30+ days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I -Heart Institute, Cheng Lab
- Los Angeles, CA
- 30+ days ago
- Los Angeles, CA
- 30+ days ago
Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events...
Clinical Research Specialist I - Gastroenterology and Hepatology Division/Department of Medicine
- Los Angeles, CA
- 10 hours ago
- Los Angeles, CA
- 10 hours ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Experienced CRA (CRA II, Sr. CRA & Principal CRA) - Ontario, Canada
- Toronto, ON
- 2 days ago
- Toronto, ON
- 2 days ago
Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts....
Summary: SystImmune is seeking a high quality, ambitious and experienced Senior Clinical Research Associate (CRA) to support SystImmune's clinical trials. The Sr....
Demonstrates competence in Good Clinical Practice (GCP) guidelines, Federal Regulations that govern and conduct human subjects research and the NYU IRB policies and procedures related to Human Subjects...
Salary Range $114,100.00 - $211,900.00 Skills Desired Budget, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data...
Remote Workresearch associate, CRA, CTA, clinical trial assistant, research associate, research assistant, research, REDCap, medidata, RAVE, EDC, electronic data capture, CTMS, clinical trial management system...
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs Nationwide
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates 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
- Consumer Lending
- Mortgage Lending
- FHLMC
- Federal National Morgage Association
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Institutional Review Board
- ICH GCP
- Sample Preparation
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Good Clinical Practice
- Gene Therapy
- ICH Guidelines
- Cancer Research
- Drug Development
- Scientific Research
- Site Management
- Pharmacovigilance
- Biotechnology
- Clinical Trials
- Neuroscience
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Health Care
- Affirmative Action
- Collections
- Investigation
- Written Communication
- Auditing
- Documentation
- Data Entry
- Collaboration
- Reporting
- Education Experience
- Microsoft PowerPoint
- Regulations
- Policy Development
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Teamwork
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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