Clinical Project Manager Jobs in California
A Clinical Project Manager in the biotechnology industry has the dynamic role of overseeing and orchestrating clinical trials. This includes developing trial protocols, coordinating with various departments and stakeholders, ensuring compliance with regulations, managing budgets, ensuring data accuracy, and liaising with regulatory authorities. This role is critical to ensuring the successful completion and analysis of clinical trials, which contribute to the development and approval of new biotechnology products. A Clinical Project Manager is also responsible for identifying and mitigating risks that could disrupt the trial timeline or compromise the data's validity.
For this role, a strong background in clinical trials, research, biotechnology, and project management is essential. A degree in life sciences or a related field is generally required, with advanced degrees or clinical research certifications being preferred. Key skills include attention to detail, problem-solving, leadership, and excellent communication skills. Certification as a Project Management Professional (PMP) can be beneficial. Prior to this role, an individual may have worked as a Clinical Trial Coordinator, Clinical Research Associate, or even as a Biostatistician, gaining valuable hands-on experience in clinical trials and research.
Patient Recruitment: Collaborate with recruitment teams to optimize patient recruitment strategies and ensure the timely enrollment of eligible study participants....
- San Francisco, CA
- 9 hours ago
- San Francisco, CA
- 9 hours 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...
Clinical Trial Participant Recruitment Project Manager
- San Diego, CA
- 16 hours ago
- San Diego, CA
- 16 hours ago
Experience applying policies and procedures, with some familiarity with ICH-GCP guidelines and working knowledge of FDA guidance documents....
Senior Clinical Research Coordinator - Gastrointestinal Medical Oncology Program
- San Francisco, CA
- 17 hours ago
- San Francisco, CA
- 17 hours ago
In-depth knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures....
Contract- Assistant Clinical Research Coordinator (Pasadena, CA)
- Pasadena, CA
- 18 hours ago
- Pasadena, CA
- 18 hours ago
the coordination and execution of clinical trials by assisting with patient recruitment, data collection, and regulatory compliance....
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital....
Cancer Clinical Research Coordinator 2 Hematology (Hybrid)
- Palo Alto, CA
- 18 hours ago
- Palo Alto, CA
- 18 hours ago
Ensure Institutional Review Board renewals are completed.Hybrid work agreement. *- Other duties may also be assigned....
Cancer Clinical Research Coordinator 2 GI (Hybrid)
- Palo Alto, CA
- 18 hours ago
- Palo Alto, CA
- 18 hours ago
Ensure Institutional Review Board renewals are completed.Hybrid work agreement. * - Other duties may also be assigned....
Cancer Clinical Research Coordinator 2 Pediatric Oncology (Hybrid)
- Palo Alto, CA
- 18 hours ago
- Palo Alto, CA
- 18 hours ago
Ensure Institutional Review Board renewals are completed.Hybrid work agreement. * - Other duties may also be assigned....
Clinical Research Coordinator 2 Pediatric Hematology (Hybrid)
- Palo Alto, CA
- 18 hours ago
- Palo Alto, CA
- 18 hours ago
Review Board requirements, and Good Clinical Practices.Knowledge of medical terminology....
Cancer Lead Clinical Research Coordinator 3 - Radiation Oncology (Hybrid)
- Stanford, CA
- 18 hours ago
- Stanford, CA
- 18 hours ago
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Cancer Clinical Research Coordinator 2 Hematology
- Stanford, CA
- 21 hours ago
- Stanford, CA
- 21 hours ago
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Cancer Clinical Research Coordinator 2 Pediatric Oncology
- Stanford, CA
- 21 hours ago
- Stanford, CA
- 21 hours ago
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
Cancer Clinical Research Coordinator 2 GI Oncology
- Stanford, CA
- 21 hours ago
- Stanford, CA
- 21 hours ago
Experience 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 2 Pediatric Hematology
- Stanford, CA
- 21 hours ago
- Stanford, CA
- 21 hours ago
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
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
- Report Generation
- ICH GCP
- Institutional Review Board
- Study Management
- Clinical Monitoring
- Biomarkers
- Genomics
- Clinical Trial Management System
- Cancer Research
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Biostatistics
- Scientific Research
- Specimen Processing
- Drug Development
- Site Management
- Medical Writing
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- Oncology
- Medical Device Sales
- 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
- Documentation
- Quality Assurance
- Collaboration
- Interpersonal Skills
- 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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