Clinical Coordinator Jobs in California, MD
A Clinical Coordinator in the Biotechnology industry is responsible for overseeing clinical trials and research projects from initiation to completion. They are tasked with planning, implementing, and managing all aspects of the trials, which includes setting up protocols, complying with regulations, and ensuring the safety and ethical treatment of participants. Additionally, they may also play a role in data analysis, compile reports and findings, and liaise with other professionals in the industry such as scientists, doctors, and administrators.
Key skills required for a Clinical Coordinator include strong organizational and leadership skills, excellent communication abilities, and an acute attention to detail. They must also have a solid understanding of medical terminology, clinical research processes, and regulatory guidelines. A degree in a relevant field such as biology, chemistry, or medical science is required, as well as a minimum of a few years of experience in clinical research. Prior certifications such as Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) can be beneficial. Before becoming a Clinical Coordinator, a professional might have served roles such as a Clinical Research Associate, Clinical Trial Assistant, or a Medical Laboratory Technologist.
, including roles in clinical data management and/or clinical data entry....
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Salary for Clinical Coordinator Jobs in California, MD
Required or preferred licenses and certifications for Clinical Coordinator positions.
Highest Education Level
Clinical Coordinators in California, MD offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Coordinator position
- Microsoft Access
- Adobe Acrobat
- Estimating
- Resolution
- Data Analytics
- Bash
- User Acceptance Testing
- Database Design
- Budgets
- Specifications
- Image Processing
- Microsoft Power BI
- TensorFlow
- Data Quality
- ICH GCP
- Institutional Review Board
- Biomarkers
- Clinical Data Management
- Proteomics
- ICH Guidelines
- Cancer Research
- Biostatistics
- Bioinformatics
- Drug Development
- Biology
- Chemical Characterization
- Epidemiology
- Hematology
- Clinical Trials
- Biotechnology
- Clinical Operations
- Clinical Research
- Validation
- Oncology
- FDA Regulations
- Medical Device Sales
- Statistical Analysis System
- Data Collection
- Standard Operating Procedures
- Data Management
- Statistics
- Computer Programming
- Affirmative Action
- Collections
- Auditing
- Written Communication
- Data Analysis
- Documentation
- Quality Assurance
- Collaboration
- Data Entry
- Bachelor's Degree
- Reporting
- Regulations
- Project Management
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Staff Supervision
- Organization
- Computer Skills
- Leadership
- Communication Skills
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