Clinical Research Associate Jobs in Louisiana
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.
Associate Clinical Research Coordinator - Biorepository Unit - Full Time
- New Orleans, LA
- 13 days ago
- New Orleans, LA
- 13 days ago
Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines. Performs other related duties as required....
LSU Health Sciences Center, Department of Surgery in New Orleans is seeking a research Clinical Trial Coordinator 1, 2, or 3....
Bachelor's degree in other area will be considered with additional three years of research or clinical trial experience in a hospital/clinic/academic setting....
Posting Details Posting Summary Functional Position TitleRN CLINICAL TRIALS COORDINATOR 3 Position Number00036116 Appointment TypeRegular Location-CityNew Orleans School/DivisionEXECUTIVE MANAGEMENT...
Under minimal supervision from the Section Chief, incumbent is responsible for the successful completion of all actions in accordance with approved protocols related to patient activities in...
The Clinical Trials Coordinator 3 will work collectively within a multidisciplinary clinical/research team to ensure that all aspects of patient management are executed both timely and accurately....
Assist with maintaining all site logs Assist with inventory and ordering equipment and supplies Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials....
Associate Clinical Research Coordinator - Transplant/Hepatology
- New Orleans, LA
- 90+ days ago
- New Orleans, LA
- 90+ days ago
Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines....
Remote WorkThe Clinical Trials Coordinator 2 will work collectively within a multidisciplinary clinical/research team to ensure that all aspects of patient management are executed both timely and accurately....
The RN Clinical Trials Coordinators (RN CTC) will coordinate, manage, and assist physicians in enrolling and monitoring patients on all Phase I drug-industry sponsored and the NCI-funded clinical trials...
Demographic Data for Louisiana
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Louisiana
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Louisiana 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
- Federal National Morgage Association
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Drug Development
- Biology
- DNA Isolation
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Standard Operating Procedures
- Patient Care
- Technical Writing
- Data Management
- Collections
- Military Background
- Auditing
- High School Diploma
- Investigation
- Written Communication
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Education Experience
- Bachelor's Degree
- Inventory Management
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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