Clinical Research Manager Jobs in San Diego, CA
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.
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)....
Project Manager - Life Sciences & Technology (California)
- San Diego, CA
- 3 days ago
- San Diego, CA
- 3 days ago
Description The Life Sciences & Technology Project Manager will lead and motivate a team in the day-to-day management of projects in the pharmaceutical, biotechnology, animal health and medical...
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
- 9 days ago
- San Diego, CA
- 9 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
- 14 days ago
- San Diego, CA
- 14 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....
Assure clinical studies are compliant with ICH/GCP and other regulations as appropriate....
Remote WorkAssure clinical studies are compliant with ICH/GCP and other regulations as appropriate....
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 Workprocedures (SOPs), ICH-GCP and applicable regulatory requirements....
Conduct 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....
Demographic Data for San Diego, CA
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Salary for Clinical Research Manager Jobs in San Diego, CA
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research 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 Research Manager position
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Genomics
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Scientific Research
- Specimen Processing
- Drug Development
- Urine Testing
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Medical Terminology
- Collections
- Quality Control
- Auditing
- Investigation
- Written Communication
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Education Experience
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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