Clinical Trial Manager Jobs in California
A Clinical Trial Manager in the biotechnology industry oversees the planning, implementation, and completion of clinical trials. They are crucial in ensuring that trials are conducted in a way that ensures patient safety, data integrity, and regulatory compliance. They manage budgets, timelines, resources, vendors, and staff involved in the clinical trial, and also handle data management and reporting. They are also responsible for protocol development, site management, and monitoring the study's progress by coordinating with the clinical research associates.
Key skills for a Clinical Trial Manager include strong leadership, project management, and communication abilities. They should also be proficient in medical terminology and have a strong understanding of Good Clinical Practices (GCP), as well as FDA and ICH regulations. A degree in life sciences, nursing or related field, certification like Certified Clinical Research Professional (CCRP) or Certified Clinical Data Manager (CCDM) are often required. Prior roles before becoming a Clinical Trial Manager might include Clinical Research Associate, Clinical Data Coordinator, or Clinical Project Coordinator.
Clinical Research Coordinator I - Heart Institute, Cheng Lab
- Los Angeles, CA
- 1 day ago
- Los Angeles, CA
- 1 day ago
Review Board (IRB)....
Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law....
Clinical Research Coordinator I - Pulmonary Research Program/Lung Institute
- Los Angeles, CA
- 1 day ago
- Los Angeles, CA
- 1 day ago
Review Board (IRB)....
Sr. Project Manager Who we are: At CitiusTech, we constantly strive to solve the industry's greatest challenges with technology, creativity, and agility. With over 8,500 healthcare technology...
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating...
CITI At least 6 years experience managing clinical trials Previous experience as a Clinical Research Coordinator or similar role Knowledge of clinical development processes and compliance management...
Update study and patient records in the University approved Clinical Trial Management System (VELOS) on a consistent basis. Other duties assigned as needed....
Program Manager, Clinical Research Operations - Hybrid/Remote - Remote - Nationwide
- Sacramento, CA
- 1 day ago
- Sacramento, CA
- 1 day ago
Working knowledge of FDA and/ or EMA Regulations, ICH Guidelines, 510k guidelines, and GCPs governing the conduct of clinical trials preferred. Experience with FDA-regulated devices preferred....
Interns will be introduced to the lifecycle and execution of clinical studies in accordance with CHOC policies and procedures, ICH/GCP, and FDA guidelines....
Assistant Clinical Research Coordinator/ Clinical Research Coordinator
- Davis, CA
- 2 days ago
- Davis, CA
- 2 days ago
In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support...
Prepare and submit regulatory documents, including Institutional Review Board (IRB) submission....
Experience with Clinical Trial Audit activities. Working knowledge of ICH/GCP guidelines. Effective written and verbal communication skills....
Clinical Research Coordinator (2 Years Fixed Term) Stanford University
- Stanford, CA
- 3 days ago
- Stanford, CA
- 3 days ago
Prepare regulatory submissions, and ensure institutional Review Board renewals are completed....
Clinical Research Coordinator (2 Years Fixed Term)
- Palo Alto, CA
- 3 days ago
- Palo Alto, CA
- 3 days ago
Prepare regulatory submissions, and ensure institutional Review Board renewals are completed.Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents,...
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Title Synonyms
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Salary for Clinical Trial Manager Jobs in California
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in California offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial 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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