Clinical Trial Manager Jobs in Louisiana
A Clinical Trial Manager in the biotechnology industry oversees the planning, implementation, and completion of clinical trials. They are crucial in ensuring that trials are conducted in a way that ensures patient safety, data integrity, and regulatory compliance. They manage budgets, timelines, resources, vendors, and staff involved in the clinical trial, and also handle data management and reporting. They are also responsible for protocol development, site management, and monitoring the study's progress by coordinating with the clinical research associates.
Key skills for a Clinical Trial Manager include strong leadership, project management, and communication abilities. They should also be proficient in medical terminology and have a strong understanding of Good Clinical Practices (GCP), as well as FDA and ICH regulations. A degree in life sciences, nursing or related field, certification like Certified Clinical Research Professional (CCRP) or Certified Clinical Data Manager (CCDM) are often required. Prior roles before becoming a Clinical Trial Manager might include Clinical Research Associate, Clinical Data Coordinator, or Clinical Project Coordinator.
specific regard to protocol timelines Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials....
Clinical Research Coordinator II - Medically Associated Science & Technology (MAST) Program
- Central, LA
- 6 days ago
- Central, LA
- 6 days ago
Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law....
Clinical Research Coordinator - Multispecialty Surgery
- New Orleans, LA
- 16 days ago
- New Orleans, LA
- 16 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
- 16 days ago
- New Orleans, LA
- 16 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....
Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines....
Remote WorkClinical 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...
Responsibilities Duties/Responsibilities: Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity's SOPs Implement and coordinate assigned clinical...
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...
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Title Synonyms
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Salary for Clinical Trial Manager Jobs in Louisiana
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Louisiana offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Biomarkers
- Cancer Research
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Scientific Research
- Specimen Processing
- Drug Development
- Biology
- Urine Testing
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- Oncology
- Medical Device Sales
- FDA Regulations
- Phlebotomy
- Data Collection
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Medical Terminology
- Collections
- Quality Control
- Military Background
- Auditing
- Investigation
- Presentation
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Education Experience
- Bachelor's Degree
- Data Entry
- 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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