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.
Manager, Clinical Research Data Systems & Analytics Oncology
- Ochsner Clinic Foundation
- New Orleans, LA
- 1 day ago
- New Orleans, LA
- 1 day ago
The Clinical Research Data Systems Manager Oncology Clinical Trials provides strategic leadership, technical expertise, and operational oversight for research systems, clinical trial data infrastructure...
In PersonAbility to evaluate and implement clinical trials....
In Person- Baton Rouge General
- Baton Rouge, LA
- 8 days ago
- Baton Rouge, LA
- 8 days ago
, and cross-functional collaboration, while ensuring all activities are conducted in accordance with Good Clinical Practice (GCP) guidelines and applicable regulatory requirements....
In PersonSenior Clinical Project Manager
- Tulane University
- New Orleans, LA
- 13 days ago
- New Orleans, LA
- 13 days ago
The Clinical research Project Manager is required to have an advanced knowledge of protocol requirements and good clinical practices as set forth by federal regulations....
In PersonClinical Research Coordinator - Biorepository Unit - Full Time
- Ochsner Clinic Foundation
- New Orleans, LA
- 15 days ago
- New Orleans, LA
- 15 days ago
Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines....
In Person Full TimeSenior Clinical Research Coordinator
- Tulane University
- New Orleans, LA
- 17 days ago
- New Orleans, LA
- 17 days ago
As 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....
In PersonClinical Research Coordinator II
- Tulane University
- New Orleans, LA
- 17 days ago
- New Orleans, LA
- 17 days ago
As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor....
In PersonClinical Research Coordinator I
- Tulane University
- New Orleans, LA
- 17 days ago
- New Orleans, LA
- 17 days ago
As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor....
In PersonSenior Clinical Research Manager - Onsite
- XOM Medtronic Xomed, LLC
- Lafayette, LA
- 23 days ago
- Lafayette, LA
- 23 days ago
Reporting to the Vice President of Clinical Research & Medical Science (CRMS), you will lead and manage a high-performing, experienced Clinical Research team for the Ear, Nose & Throat (ENT) Operating...
In PersonClinical Research Coordinator - Multispecialty Surgery
- Ochsner Clinic Foundation
- New Orleans, LA
- 28 days ago
- New Orleans, LA
- 28 days ago
Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines....
In Person- C0007 Franciscan Health Lafayette
- Lafayette, LA
- 28 days ago
- Lafayette, LA
- 28 days ago
Conduct clinical trials that involve human subjects, according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines....
In Person- Mens Health Foundation
- Central, LA
- 30+ days ago
- Central, LA
- 30+ days ago
Computer Skills: Working knowledge of MS Office Suite, electronic Health Records (EHR), Clinical Trial Management Systems (CTMS), and Electronic Data Capture (EDC)....
In Person- Medix Staffing Solutions
- Kenner, LA
- 45+ days ago
- Kenner, LA
- 45+ days ago
Responsibilities Oversee and manage all phases of clinical trials, including recruiting participants, coordinating schedules, and ensuring consistent follow-up for seamless execution Evaluate and confirm...
In Person- Tandem Clinical Research
- Covington, LA
- 45+ days ago
- Covington, LA
- 45+ days ago
Key Responsibilities Study Management & Coordination Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out....
In PersonClinical Research Coordinator II (30720)
- GI Alliance
- Lafayette, LA
- 45+ days ago
- Lafayette, LA
- 45+ days ago
The CRC supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study....
In PersonDemographic Data for Louisiana
Moving to Louisiana? Find some basic demographic data about Louisiana below.
Clinical Trial Manager Online Courses and Training Opportunities
Title Synonyms
Users interested in this job title also searched for the following job titles
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
- Budgets
- Good Clinical Practice
- ICH Guidelines
- Study Management
- Institutional Review Board
- Clinical Monitoring
- Biomarkers
- ICH GCP
- Clinical Trial Management System
- Drug Development
- Clinical Data Management
- Scientific Research
- Gene Therapy
- Cancer Research
- Biology
- Site Management
- Clinical Trials
- Specimen Collection
- Clinical Operations
- Clinical Research
- Biotechnology
- Neuroscience
- Neurology
- Medical Device Sales
- Venipuncture
- FDA Regulations
- Oncology
- Data Collection
- Standard Operating Procedures
- Patient Care
- Phlebotomy
- Data Management
- Medical Terminology
- Health Care
- Collections
- Quality Control
- Auditing
- Written Communication
- Investigation
- Documentation
- Interpersonal Skills
- Implementation
- Reporting
- Data Entry
- Collaboration
- Education Experience
- Bachelor's Degree
- Regulations
- Research Skills
- Microsoft Excel
- Microsoft Office
- Project Management
- Problem Solving
- Staff Supervision
- Scheduling
- Leadership
- Communication Skills
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