Clinical Trial Manager Jobs in San Diego, CA
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.
Sr. Project Manager Employer Syner-G BioPharma Group Location San Diego, California, United States Start date Jun 26, 2025 categoriesView less categories Job Details Company Job Details COMPANY...
Remote Workmaintained and the research is conducted in accordance with Good Clinical Practice Guidelines....
Minimum of 2 to 4 years of monitoring experience in a clinical research environment and administrative Institutional Review Board (IRB) experience....
The Clinical Trial Manager (CTM) is responsible for managing and supporting clinical trials in compliance with applicable regulations, ICH/GCP guidelines, and standard operating procedures (SOPs)....
Proactively stay abreast of the latest regulations and GCP (Good Clinical Practice) Support management of CRO and/or other outside clinical vendors. Co-manage study timelines and budgets....
Senior Contracts Manager, Clinical Research & Development
- San Diego, CA
- 18 days ago
- San Diego, CA
- 18 days ago
Trial Agreements for US and ex-US clinical research sites, CMC clinical and commercial supply agreements, agreements for Investigator Initiated Studies, and other life sciences R&D agreements....
Cardiovascular Clinical Research Coordinator (RN or LVN)
- San Diego, CA
- 22 days ago
- San Diego, CA
- 22 days ago
GCP (Good Clinical Practice) Certification within the last two years (preferred)....
Perform all duties and responsibilities in accordance with CFR, GCP/ICH Guidelines, SOPs, and other applicable guidelines....
The Clinical Trial Manager will interact internally and externally with members of the cross-functional study team....
Remote WorkPosition Summary: The Senior Clinical Trial Manager is responsible for managing the execution of clinical studies and data collection....
Remote WorkDrug Development knowledge with understanding of other functions relevant to the position which may include: Discovery, Preclinical, Clinical Research, Clinical Operations, Manufacturing, Commercial...
Remote WorkConduct and manage clinical trials in accordance with the study protocol guidelines and internal SOP's....
maintained and the research is conducted in accordance with Good Clinical Practice Guidelines....
The Clinical Research Coordinator II will help ensure the success of clinical trials and research projects at NHRC....
Ensure compliance with corporate SOPs and health authority, ICH/GCP, and local regulations and guidelines....
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Salary for Clinical Trial Manager Jobs in San Diego, CA
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in San Diego, CA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Report Generation
- ICH GCP
- Institutional Review Board
- Study Management
- Clinical Monitoring
- Genomics
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Biostatistics
- Scientific Research
- Specimen Processing
- Urine Testing
- Drug Development
- Medical Writing
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- Oncology
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- 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
- Policy Development
- Bachelor's Degree
- Regulations
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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