Clinical Research Manager Jobs in Alaska
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.
environment. + Strong scientific and clinical research knowledge is required. + Strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus...
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Title Synonyms
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Salary for Clinical Research Manager Jobs in Alaska
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research Managers in Alaska offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Manager position
- Institutional Review Board
- ICH GCP
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Biomarkers
- Clinical Data Management
- Good Clinical Practice
- Gene Therapy
- ICH Guidelines
- Cancer Research
- Medical Affairs
- Drug Development
- Biology
- Scientific Research
- Site Management
- Medical Writing
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Medical Device Sales
- Public Health
- Data Collection
- Patient Care
- Standard Operating Procedures
- Phlebotomy
- Data Management
- Medical Terminology
- Health Care
- Affirmative Action
- Collections
- Quality Control
- Military Background
- Investigation
- Written Communication
- Auditing
- Documentation
- Quality Assurance
- Data Entry
- Collaboration
- Reporting
- Education Experience
- Bachelor's Degree
- Regulations
- Policy Development
- Project Management
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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