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.
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 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
- 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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