Clinical Coordinator Jobs in California
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.
Mentor junior team members in the roles and responsibilities of the Clinical Data Management Analyst. Required Qualifications B.S. in Computer Science, Life Sciences or Technical Field....
research is required A strong background in Electrophysiology and/or Cardiology is required....
research is required A strong background in Electrophysiology and/or Cardiology is required....
Ensure CDM activities are performed in compliance with Good Clinical Practice, ICH Guidelines, Biogen SOPs, Job Aids, regulatory guidelines, and study specific plans....
Strong knowledge of clinical research processes, FDA & ICH guidelines, GCP, GCDMP, and CDISC standards. Demonstrated experience in CRO and vendor oversight....
Clinical Practices (GCP), FDA regulations and guidelines, and international regulatory requirements/guidelinesSolid understanding of Biopharmaceutical/Healthcare ComplianceQualified candidates should...
Knowledge of data collection best practices for clinical trials; Knowledge of global clinical operations....
Pay rate: $25 - $30/hr. Responsibilities: Manage agreements from start to finish including logging and updating contract management system for agreements. Ensuring that agreements are reviewed in...
Job Requirement Clinical Data Manager Clinical Data Management Project Management Clinical Operations CDISC ADaM STDM CRF Medidata Clinical Data Manager Clinical Data Management Project Management Clinical...
Knowledge of data collection best practices for clinical trials. Knowledge of global clinical operations....
Requires solid knowledge of clinical data management principles, clinical trials process and regulatory requirements. Good working knowledge of ICH, FDA, and GCP regulations and guidelines....
Case Report Form (CRF), Clinical Assessment, Clinical Data, Clinical Data Management, Clinical Support, Clinical Trial, Communication Skills....
ICH, GCP, HIPAA). Strong interpersonal communication (written and verbal) and organizational skills....
research, clinical trials, and longitudinal data sets....
Cancer Clinical Research Data Manager Gastrointestinal Oncology
- Stanford, CA
- 90+ days ago
- Stanford, CA
- 90+ days ago
Previous experience with clinical trials, data management....
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Salary for Clinical Coordinator Jobs in California
Required or preferred licenses and certifications for Clinical Coordinator positions.
Highest Education Level
Clinical Coordinators in California offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Coordinator position
- Verbal Communication
- Affirmative Action
- Resolution
- Pivot Tables
- IBM SPSS Statistics
- Data Analytics
- User Acceptance Testing
- Data Migration
- Computer Science
- Specifications
- Data Visualization
- Microsoft Power BI
- Management Information Systems
- Data Quality
- ICH GCP
- Genomics
- Clinical Trial Management System
- Biomarkers
- Cancer Research
- Clinical Data Management
- Proteomics
- ICH Guidelines
- Good Clinical Practice
- Next-Generation Sequencing
- Biostatistics
- Drug Development
- Biology
- Bioinformatics
- Biotechnology
- Scientific Writing
- Clinical Trials
- Clinical Research
- Clinical Operations
- Validation
- Oncology
- FDA Regulations
- Statistical Analysis System
- Data Collection
- Public Health
- Standard Operating Procedures
- Patient Care
- Data Management
- Computer Programming
- Collections
- Auditing
- Data Analysis
- Collaboration
- Documentation
- Data Entry
- Reporting
- Critical Thinking
- Regulations
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Leadership
- Communication Skills
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