Clinical Research Manager Jobs in New Orleans, LA
A Clinical Research Manager plays a pivotal role in the biotechnology industry by overseeing and managing clinical trials. They are responsible for creating and implementing trial protocols, ensuring compliance with legal and ethical standards, coordinating with various internal and external stakeholders, and overseeing data collection, management, and analysis. They also monitor the progress of clinical studies and ensure they are completed on time and within budget, while maintaining patient safety and data integrity.
Key skills and certifications for this role include a robust knowledge of Good Clinical Practice (GCP) guidelines, strong analytical and project management skills, and excellent communication abilities. A Clinical Research Manager may also need certifications such as Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC). Prior to becoming a Clinical Research Manager, an individual might have roles such as Clinical Research Associate or Clinical Research Coordinator, which provide the essential experience in clinical trial conduct and management.
Clinical Research Coordinator - Multispecialty Surgery
- New Orleans, LA
- 20 days ago
- New Orleans, LA
- 20 days ago
**Knowledge Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Working knowledge of ICH guidelines for ethical conduct of research. + Strong critical...
Remote WorkClinical Research Coordinator - Neurosciences - On Site
- New Orleans, LA
- 21 days ago
- New Orleans, LA
- 21 days ago
**Knowledge Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Working knowledge of ICH guidelines for ethical conduct of research. + Strong critical...
Remote WorkAs the primary resource for the protocol, the Senior Clinical Research Coordinator acts as a liaison between the patient, staff, investigator, collaborators, Institutional Review Board and sponsor....
Clinical Research Coordinator I, II & III (Baton Rouge)
- New Orleans, LA
- 30+ days ago
- New Orleans, LA
- 30+ days ago
Research and associated regulationsPreferred Spanish language fluency-oral and written Level II Knowledge of IRB submission process and requirements Knowledge of good clinical practices as set forth...
As the primary resource for protocols, the Clinical Research Coordinator I acts as a liaison between the patient, investigator, Institutional Review Board and sponsor....
Research 3 years Master's degree Project management Bachelor's degree Doctor of Philosophy Clinical trials Good Clinical Practice CCRP Training & development Senior level Leadership Communication skills...
As the primary resource for the protocol, the Senior Clinical Research Coordinator acts as a liaison between the patient, investigator, collaborators, Institutional Review Board and sponsor....
Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical...
Bachelor's degree or RN with current LA licensure at the time of hire Two years professional clinical research work experience, or in lieu of that and advanced degree such as Masters degree in Clinical...
Demographic Data for New Orleans, LA
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Salary for Clinical Research Manager Jobs in New Orleans, LA
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research Managers in New Orleans, LA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Manager position
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Genomics
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Scientific Research
- Specimen Processing
- Drug Development
- Urine Testing
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Medical Terminology
- Collections
- Quality Control
- Auditing
- Investigation
- Written Communication
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Education Experience
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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