Clinical Research Manager Jobs in Oregon
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 is required to use Personal Protective Equipment (gloves, masks, etc.) as required to maintain a safe and healthy clinical research environment....
The CRC provides support in accordance with our policies and procedures, hospital regulations and the Code of Federal Regulation and Good Clinical Practice guidelines....
Demographic Data for Oregon
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Clinical Research Manager Online Courses and Training Opportunities
Title Synonyms
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Salary for Clinical Research Manager Jobs in Oregon
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research Managers in Oregon offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Manager position
- Report Generation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Biostatistics
- Scientific Research
- Specimen Processing
- Urine Testing
- Drug Development
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- Oncology
- Medical Device Sales
- FDA Regulations
- Phlebotomy
- Public Health
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Health Care
- Medical Terminology
- Collections
- Military Background
- Auditing
- Investigation
- Education Experience
- Interpersonal Skills
- Quality Assurance
- Collaboration
- 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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