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.
Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures...
Clinical Research Assistant I Boston Children's Hospital
- Boston, MA
- moments ago
- Boston, MA
- moments ago
Coordinates and prepares the necessary documentation for Institutional Review Board IRB and Committee on Clinical Investigations CCI submissions, together with the Private Investigator of the study....
Clinical Research Associate I ? (Hybrid) Cedars-Sinai Medical Center
- Beverly Hills, CA
- moments ago
- Beverly Hills, CA
- moments ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Ensure adherence to Good Clinical Practices, Industry standards, standard operating procedures and to all other regulatory and quality standards in conducting Lingo Clinical research and development...
Clinical Research Associate - IMM/Cross TA - Chicago, IL (Field Based)
- Chicago, IL
- 12 hours ago
- Chicago, IL
- 12 hours ago
As a Clinical Research Associate you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence....
Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Cancer Center-Res Fac **Work Type:** Full Time (Total FTE between 0.9 and 1.0)...
Coordinates and prepares the necessary documentation for Institutional Review Board IRB and Committee on Clinical Investigations CCI submissions, together with the Private Investigator of the study....
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...
If you are a current FIB employee, please apply through the Career Worklet in the Employee Portal. This position can be located at Boise, ID, Omaha, NE, Sioux Falls, SD and Great West Center in...
A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation's top public...
Clinical Research Associate /Clinical Trial Manager (Hybrid Role) - TEMP To PERM
- New York, NY
- 20 hours ago
- New York, NY
- 20 hours ago
Job Overview: The Clinical Research Associate (CRA)/Clinical Trial Manager (CTM) is responsible for providing oversight of the Sponsor's outsourced Contracted Research Organizations (CRO) clinical trial...
Key Responsibilities Coordinates and prepares the necessary documentation for Institutional Review Board IRB submissions, together with the Principal Investigators....
Liaises with Legal to secure confidentiality agreements, master service agreements, clinical trial agreements as appropriate....
The Clinical Research Associate II/Site Monitor II will be responsible for data integrity, data quality and ensuring compliance with International Conference on Harmonization and Good Clinical Practice...
Remote WorkClinical Trial Management System). + Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts. +...
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
- Mortgage Lending
- 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
- Biology
- Drug Development
- Pharmacovigilance
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Technical Writing
- Health Care
- Collections
- Process Improvement
- Auditing
- Investigation
- Written Communication
- Presentation
- Education Experience
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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