... Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused ... Essential job duties include, but are not limited to: * Assist the Principal Investigator in ...
... Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused ... Essential job duties include, but are not limited to: * Assist the Principal Investigator in ...
Clinical Project Manager
Los Angeles, CA · On-site
... Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused ... Essential job duties include, but are not limited to: * Assist the Principal Investigator in ...
Clinical Project Manager
Los Angeles, CA · On-site
... Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused ... Essential job duties include, but are not limited to: * Assist the Principal Investigator in ...
... Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused ... Essential job duties include, but are not limited to: * Assist the Principal Investigator in ...
... Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused ... Essential job duties include, but are not limited to: * Assist the Principal Investigator in ...
Associate Clinical Project Manager / Clinical Project Manager
San Diego, CA · On-site
$80K - $100K/yr
Senior Director, Clinical Operations and Project Management Hours: Full-Time Location: Onsite or ... In general, you will assist the clinical operations and program management leadership teams with ...
Quick apply
Associate Clinical Project Manager / Clinical Project Manager
San Diego, CA · On-site
$80K - $100K/yr
Senior Director, Clinical Operations and Project Management Hours: Full-Time Location: Onsite or ... In general, you will assist the clinical operations and program management leadership teams with ...
Project Management
La Jolla, CA · On-site
Qualifications At least 5 years clinical project assistant experience required Additional Information Best Regards, Anuj Mehta 973-967-3402
Project Management
La Jolla, CA · On-site
Qualifications At least 5 years clinical project assistant experience required Additional Information Best Regards, Anuj Mehta 973-967-3402
Project Assistant
Los Angeles, CA · On-site
$25.96/hr
... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Job Function The Project Assistant will be in charge of pre/post-processing raw imaging data (MRI ...
Project Assistant
Los Angeles, CA · On-site
$25.96/hr
... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Job Function The Project Assistant will be in charge of pre/post-processing raw imaging data (MRI ...
Project Assistant
Marina Del Rey, CA · On-site
$25.96/hr
... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Job Function The Project Assistant will be in charge of pre/post-processing raw imaging data (MRI ...
Project Assistant
Marina Del Rey, CA · On-site
$25.96/hr
... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Job Function The Project Assistant will be in charge of pre/post-processing raw imaging data (MRI ...
Project Assistant
Los Angeles, CA · On-site
$25.96/hr
... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Job Function The Project Assistant will be in charge of pre/post-processing raw imaging data (MRI ...
Project Assistant
Los Angeles, CA · On-site
$25.96/hr
... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Job Function The Project Assistant will be in charge of pre/post-processing raw imaging data (MRI ...
Must meet all requirements for CPA grade 24 position and have demonstrated proficiency in all relevant areas Provide input and assist with harmonization of Clinical Operations databases and tracking ...
Must meet all requirements for CPA grade 24 position and have demonstrated proficiency in all relevant areas Provide input and assist with harmonization of Clinical Operations databases and tracking ...
Orders and maintains inventory of clinical supplies. Orders and ships case report forms. Assists ... May assist with monitoring visits under the direct supervision of senior staff. Travel may be ...
Orders and maintains inventory of clinical supplies. Orders and ships case report forms. Assists ... May assist with monitoring visits under the direct supervision of senior staff. Travel may be ...
Interacts with various study support groups and the business unit in order to assist in clinical strategy, the development of study plans, and project deliverables. • Is also assigned to other non ...
Interacts with various study support groups and the business unit in order to assist in clinical strategy, the development of study plans, and project deliverables. • Is also assigned to other non ...
Provide input and assist with harmonization of Clinical Operations databases and tracking tools. * Assist in the maintaining clinical information and training of Clinical Operations personnel in the ...
Provide input and assist with harmonization of Clinical Operations databases and tracking tools. * Assist in the maintaining clinical information and training of Clinical Operations personnel in the ...
We are seeking a Clinical Supply Chain Project Manager to oversee clinical trial supply planning ... Key Responsibilities: * Assist in developing appropriate drug supply plans across all phases of a ...
Quick apply
We are seeking a Clinical Supply Chain Project Manager to oversee clinical trial supply planning ... Key Responsibilities: * Assist in developing appropriate drug supply plans across all phases of a ...
Clinical Trials Management Associate II
Foster City, CA · On-site
$39 - $53.25/hr
May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants. Under general supervision, participates in two or more departmental or interdepartmental ...
Clinical Trials Management Associate II
Foster City, CA · On-site
$39 - $53.25/hr
May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants. Under general supervision, participates in two or more departmental or interdepartmental ...
Clinical Trials Management Associate
Foster City, CA · On-site
$39 - $53.25/hr
May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants. Under general supervision, participates in two or more departmental or interdepartmental ...
Clinical Trials Management Associate
Foster City, CA · On-site
$39 - $53.25/hr
May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants. Under general supervision, participates in two or more departmental or interdepartmental ...
... Labs, etc. Assist in overall project tasks such as process flowcharts, Standard Operating ... Clinical Database Systems Knowledge - EDC and Paper Intermediate to Advanced level proficiency with ...
... Labs, etc. Assist in overall project tasks such as process flowcharts, Standard Operating ... Clinical Database Systems Knowledge - EDC and Paper Intermediate to Advanced level proficiency with ...
May assist with monitoring visits under the direct supervision of senior staff. * Travel may be ... clinical operating procedures is a plus. * Must be able to work both independently and as part of a ...
May assist with monitoring visits under the direct supervision of senior staff. * Travel may be ... clinical operating procedures is a plus. * Must be able to work both independently and as part of a ...
Senior Vice President, Clinical Development
San Diego, CA · On-site
$306K - $459K/yr
Develop and monitor overall clinical development budget for assigned projects; effectively manage resources, funding and expenses. * Assist with tracking and forecasting resource capacity and ...
Senior Vice President, Clinical Development
San Diego, CA · On-site
$306K - $459K/yr
Develop and monitor overall clinical development budget for assigned projects; effectively manage resources, funding and expenses. * Assist with tracking and forecasting resource capacity and ...
Senior Vice President, Clinical Development
San Diego, CA · On-site
$306K - $459K/yr
Develop and monitor overall clinical development budget for assigned projects; effectively manage resources, funding and expenses. * Assist with tracking and forecasting resource capacity and ...
Senior Vice President, Clinical Development
San Diego, CA · On-site
$306K - $459K/yr
Develop and monitor overall clinical development budget for assigned projects; effectively manage resources, funding and expenses. * Assist with tracking and forecasting resource capacity and ...
Develop and monitor overall clinical development budget for assigned projects; effectively manage resources, funding and expenses. * Assist with tracking and forecasting resource capacity and ...
Develop and monitor overall clinical development budget for assigned projects; effectively manage resources, funding and expenses. * Assist with tracking and forecasting resource capacity and ...
Clinical Project Assistant information
See California salary details
$11.39 - $12.94
1% of jobs
$12.94 - $14.49
5% of jobs
$14.49 - $16.05
15% of jobs
$16.35 is the 25th percentile. Wages below this are outliers.
$16.05 - $17.60
20% of jobs
The median wage is $18.61 / hr.
$17.60 - $19.15
14% of jobs
$19.15 - $20.70
13% of jobs
$20.70 - $22.26
7% of jobs
$22.31 is the 75th percentile. Wages above this are outliers.
$22.26 - $23.81
8% of jobs
$23.81 - $25.36
9% of jobs
$25.36 - $26.92
4% of jobs
$26.92 - $28.47
3% of jobs
$11
$19
$28
How much do clinical project assistant jobs pay per hour?
What is a clinical project assistant?
What are the key skills and qualifications needed to thrive as a clinical project assistant?
What are some common challenges faced by clinical project assistants, and how can they be managed effectively?
What is the difference between Clinical Project Assistant vs Clinical Research Coordinator?
| Aspect | Clinical Project Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health sciences or related field | Usually requires a bachelor's degree; some roles prefer certification or experience |
| Work Environment | Supports project teams in clinical trial settings, often within pharmaceutical or biotech companies | Manages and oversees clinical trials at research sites or hospitals |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, academic research centers, clinical trial sites |
| Search & Comparison Intent | High overlap in job duties and required skills, often searched together |
The Clinical Project Assistant primarily supports clinical trial projects by assisting with documentation, scheduling, and communication within the project team. In contrast, the Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites, including patient recruitment and data collection. While both roles require similar educational backgrounds and work in related environments, their responsibilities differ in scope and focus.
What are the most commonly searched types of Clinical Project jobs in California?
The most popular types of Clinical Project jobs in California are:
What cities in California are hiring for Clinical Project Assistant jobs?
Cities in California with the most Clinical Project Assistant job openings:

Full-time
Re-posted 18 days ago
Job description
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused on behavioral health, substance use, and mental health intervention development. Working under the supervision of Dr. Mark Prince, Associate Professor and Director of My Mental Health Data Analysis and Dissemination, the Clinical Project Manager will play a central role in coordinating research operations, ensuring regulatory compliance, supporting data quality and analysis, and managing project timelines, personnel, and finances for Dr. Prince's research portfolio.
The successful candidate will be motivated, proactive, resourceful, and detail-oriented, with excellent organizational and communication skills and the ability to manage complex projects in a fast-paced academic research environment. This role requires adaptability, sound judgment, and the ability to collaborate effectively with investigators, research staff, university partners, and external stakeholders.
Essential job duties include, but are not limited to:
- Assist the Principal Investigator in formulating research objectives and translating those objectives into actionable project plans, timelines, and operational workflows.
- Plan, organize, and coordinate clinical research activities to ensure studies are conducted in accordance with approved protocols, institutional policies, and sponsor requirements.
- Develop, implement, document, and communicate operating policies, procedures, and systems to support research operations and ensure consistency across projects.
- Contribute to the design and refinement of research protocols, including procedures for data acquisition, management, and quality control.
- Support data management and analytic workflows, including oversight of data quality, monitoring of analytic outputs, and preparation of technical summaries and reports.
- Conduct quality assurance reviews of research activities and protocols; identify, document, and report deviations or compliance issues, and support corrective actions as needed.
- Ensure compliance with institutional, federal, and regulatory standards, including IRB, NIH, and other sponsor requirements.
- Support preparation for audits, reviews, and inspections by accrediting or regulatory agencies.
- Directly or indirectly supervise project staff, including coordinating assignments, providing training and technical guidance, monitoring progress, and supporting performance management in accordance with university policy.
- Develops and manages program budgets in collaboration with the Principal Investigator, department, and school partners.
- Processes procurement and reimbursements; facilitates vendor contracts and payments; reconciles accounts; and prepares financial reports. Serves as a liaison with university offices, including Purchasing and Accounts Payable, to ensure accurate, timely, and compliant transactions.
- Establish and maintain professional relationships with collaborators, university partners, and external stakeholders; represent the project and department at meetings, seminars, and professional events as appropriate.
- Promote and maintain safety, security, and compliance with departmental and university procedures, including dissemination of relevant safety and security information to staff.
- Perform other related duties as assigned or requested. The University reserves the right to add or change duties at any time.
Minimum Qualifications
- Bachelor's degree or combined experience/education as substitute for minimum education
- Minimum 5 years of relevant experience in clinical research coordination, project management, or related work
Preferred Qualifications
- Master's degree
- 7 or more years of relevant experience in academic or clinical research environments
- Experience managing complex, multi-component research projects and interdisciplinary teams
Required Skills
- Strong analytical, problem-solving, and organizational skills
- Excellent verbal and written communication skills
- Demonstrated ability to manage multiple priorities, meet deadlines, and work independently
- Strong interpersonal skills with a customer service-oriented mindset
- Ability to work collaboratively with investigators, staff, and institutional partners
- Familiarity with research compliance, quality assurance, and data management processes
- Ability to follow established USC and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan.
Work Location
This position is hybrid, and the employee must report to work at the USC Health Sciences Campus in Los Angeles, CA when scheduled. Work hours and on-site days may be subject to change depending on business needs.
Compensation
The annual budgeted salary range for this position is $92,000 - $100,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.
Minimum Education: Bachelor's degreeMinimum Experience: 5 years
Minimum Field of Expertise: Degree plus postgraduate certification/licensure in specialized clinical field. Current BCLS certification. Patient care and teaching experience. Familiarity with JCAHO requirements. Experience in conducting clinical research trials.
USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to theBackground Screening Policy Appendix Dfor specific employment screen implications for the position for which you are applying.
We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email atuschr@usc.edu. Inquiries will be treated as confidential to the extent permitted by law.
- Notice of Non-discrimination
- Employment Equity
- Read USC's Clery Act Annual Security Report
- USC is a smoke-free environment
- Digital Accessibility
If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser:
https://wd5.myworkday.com/usc/d/inst/1$9925/9925$140593.htmldAbout USC Auxiliary Services
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Industry
Colleges, universities, and professional schools
Company size
1,001 - 5,000 Employees
Headquarters location
Los Angeles, CA, US
Year founded
1929