Clinical Research Associate Jobs in Houston, TX
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.
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols...
Clinical Research Specialist (Center for Innovation)
- Houston, TX
- 15 days ago
- Houston, TX
- 15 days ago
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols...
Clinical Research Specialist, Medicine - Mylonakis lab
- Houston, TX
- 18 days ago
- Houston, TX
- 18 days ago
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols...
Clinical Research Associate - Cross Therapeutic Area - Dallas, Austin, or Houston (Field Based)
- Houston, TX
- 19 days ago
- Houston, TX
- 19 days ago
Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements....
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols...
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols...
trial sites in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs to the most rigorous standards of quality and timely delivery....
Senior Research Administration Associate - Clinical Research Billing and Budgeting
- Houston, TX
- 30+ days ago
- Houston, TX
- 30+ days ago
Maintain budget section in Clinical Trial Management System (CTMS) - Generates reports. Track all revenue and expenditures related to studies in CTMS....
We are seeking an Clinical Research Associate II/Sr. to support our Clinical Operations team....
Demographic Data for Houston, TX
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Houston, TX
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Houston, TX offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Thermogravimetric Analysis
- Mortgage Lending
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Drug Development
- Centrifuge
- Biology
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Anatomy and Physiology
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Standard Operating Procedures
- Patient Care
- Technical Writing
- Data Management
- Health Care
- Collections
- Process Improvement
- Auditing
- Investigation
- Presentation
- Collaboration
- Documentation
- Quality Assurance
- Bachelor's Degree
- Data Entry
- Reporting
- Education Experience
- Regulations
- Inventory Management
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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