Clinical Research Associate Jobs in New York
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 /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...
Review Board and other agencies. + Assists with regulatory submissions, including the Protocol Review and Monitoring Committee (PRMC, the Institutional Review Board (IRB) and ancillary committees,...
We are seeking a highly organized and detail-oriented Quality Assurance Associate to support our Clinical Operations team, with a focus on Care Navigation and Employer Services. This full-time,...
Complies with Good Clinical Practice and the Code of Federal Regulations....
Manager, CRA Strategy and Program Management Within Capital One, External Affairs (EA) is an organization dedicated to delivering on Capital One's Mission by strengthening our reputation,...
Prepares and submits all necessary documents to the Clinical Science Evaluation Committee (CSEC), the Institutional Review Board (IRB) and ancillary committees.Works with the research team to facilitate...
Reports all Serious Adverse Events (SAEs) to the Institutional Review Board and other agencies, as required....
About the Role The In-House Clinical Research Associate (CRA) at Worldwide U.S....
Experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is highly desirable....
Clinical Research Associate I Title: Clinical Research Associate I Job Type: RegularCompany: Health Research, Inc....
Job Summary: Position is Project Manager for a large multi-site clinical trial. Train and oversee CRA's on the project. Clinical Site is also Coordination Center for the clinical trial....
Submit clinical trial patient data to sponsor in timely manner....
Complies with Good Clinical Practice and the Code of Federal Regulations....
Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of Orthopedic Surgery....
Job Summary: The Clinical Research Associate will help coordinate Clinical Research Studies in the Division of Pediatric Infectious Diseases....
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in New York
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in New York 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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