Clinical Trial Manager Jobs in Texas
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.
Working knowledge of clinical trials. Working knowledge of the principles of Good Clinical Practices (GCP)....
Jump-start your career as a Clinical Research Coordinator today with Medical City Fort Worth....
This position also provides guidance to department and HMRI leadership on relevant clinical trial issues and development....
Project Manager Texas Tech University United States, Texas, Lubbock Jun 13, 2025 Lubbock Project Manager 41346BR Center for BioTechnology Genomics Position Description Provides project management...
Partners and coordinates with regulatory compliance including preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety...
Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law....
This position will manage and oversee the daily operations of Phase 1 clinical trials....
Emerging understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment. Basic understanding of medical terminology....
The Senior Clinical Trial Manager will oversee the execution of clinical studies across multiple geographic regions, ensuring compliance with Good Clinical Practices, Standard Operating Procedures,...
Remote Workavailable to clinical research unit....
Serve as a resource for other clinical research professionals in all aspects of conducting a clinical trial....
Previous experience in psychiatry, neurology and oncology as a clinical trial coordination is strongly preferred. Familiarity with ethical and regulatory guidelines (e.g., IRB, GCP)....
Clinical Research Coordinator/Patient Recruitment - San Antonio, TX
- San Antonio, TX
- 10 days ago
- San Antonio, TX
- 10 days ago
Working knowledge of clinical trials. Working knowledge of the principles of Good Clinical Practices (GCP)....
Responsibilities: Administratively and clinically manage industry-sponsored clinical trials Adhere to Research SOP's, Good Clinical Practices and the study protocols Participate actively in the communication...
Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law....
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Salary for Clinical Trial Manager Jobs in Texas
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Texas 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
- Cancer Research
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Scientific Research
- Specimen Processing
- Drug Development
- Biology
- Site Management
- Specimen Collection
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- 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
- Investigation
- Auditing
- Presentation
- Collaboration
- Documentation
- Quality Assurance
- Reporting
- Interpersonal Skills
- Bachelor's Degree
- Data Entry
- Education Experience
- Regulations
- Policy Development
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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