Clinical Project Manager Jobs in California
Clinical Trial Manager, Clinical Operations (Early Phase)
- Thousand Oaks, CA
- 6 hours ago
- Thousand Oaks, CA
- 6 hours ago
Proficient knowledge of ICH GCP, CFR, and other applicable regulatory requirements for clinical trial conduct....
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Assistant Clinical Research Coordinator - Recruitment (1 Year Fixed-Term)
- Palo Alto, CA
- 7 hours ago
- Palo Alto, CA
- 7 hours ago
Position Summary: The LIFESCAPE study at Stanford is seeking an Assistant Clinical Research Coordinator (ACRC) to participate in the coordination of the LIFESCAPE clinical trial, comparing two evidence-based...
Science Project Manager & Grant Writer (Part-Time/Flexible)
- Los Angeles, CA
- 9 hours ago
- Los Angeles, CA
- 9 hours ago
Clinical study support & administration Support setup, documentation, and coordination of clinical trials and research collaborations....
What You Will Need Required Bachelors degree Minimum 6 years of clinical study management experience at the sponsor level (CRO or medical device company); site-level experience will only be considered...
Assistant Clinical Research Coordinator - Recruitment (1 Year Fixed-Term) Stanford University
- Stanford, CA
- 21 hours ago
- Stanford, CA
- 21 hours ago
Position Summary: The LIFESCAPE study at Stanford is seeking an Assistant Clinical Research Coordinator (ACRC) to participate in the coordination of the LIFESCAPE clinical trial, comparing two evidence-based...
Clinical Research Coordinator Melanoma and Cutaneous Oncology Program
- San Francisco, CA
- 1 day ago
- San Francisco, CA
- 1 day ago
Knowledge of clinical research in oncology. Knowledge and experience in managing oncology clinical trials. Membership in a clinical research professional society....
Bachelor's degree Minimum of 5 years of clinical research study management experience, Or Masters degree with a minimum of 3 years of clinical research study management experience....
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
trials in accordance with study protocols, Good Clinical Practice, Standard Operating Procedures, and applicable regulations....
Remote WorkExperience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Clinical Research Coordinator - Urology University of California San Francisco
- San Francisco, CA
- 3 days ago
- San Francisco, CA
- 3 days ago
applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance...
Cancer Clinical Research Coordinator 2 - CCT/BMT(Hybrid)
- Palo Alto, CA
- 4 days ago
- Palo Alto, CA
- 4 days ago
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Institutional Review Board ( IRB ) and Good Clinical Practice ( GCP ) compliance requirements. NIH policies and general grant-funded research operations....
Under the supervision of the Clinical Research Supervisor, Clinical Research Coordinators (CRC) support the clinical trial management of investigator-sponsored, pharmaceutical-sponsored, and/or other...
Demographic Data for California
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Title Synonyms
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Salary for Clinical Project Manager Jobs in California
Required or preferred licenses and certifications for Clinical Project Manager positions.
Highest Education Level
Clinical Project Managers in California offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Project Manager position
- Clinical Monitoring
- Study Management
- Cancer Research
- Clinical Data Management
- ICH GCP
- Gene Therapy
- Genomics
- Clinical Trial Management System
- Drug Discovery
- Urine Testing
- Scientific Research
- ICH Guidelines
- Pharmacovigilance
- Specimen Processing
- Institutional Review Board
- Drug Development
- Good Clinical Practice
- Clinical Operations
- Biotechnology
- Oncology
- Medical Device Sales
- Clinical Trials
- Patient Care
- Clinical Research
- Phlebotomy
- Public Health
- FDA Regulations
- Data Collection
- Standard Operating Procedures
- Data Management
- Medical Terminology
- Health Care
- Collections
- Written Communication
- Auditing
- Collaboration
- Documentation
- Reporting
- Investigation
- Inventory Management
- Interpersonal Skills
- Data Entry
- Education Experience
- Quality Assurance
- Policy Development
- Problem Solving
- Bachelor's Degree
- Project Management
- Regulations
- Microsoft Office
- Microsoft Excel
- Time Management
- Computer Skills
- Research Skills
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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