Clinical Project Manager
$92k - $100kUniversity of Southern California
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. The Clinical Project Manager will work under the supervision of Dr. Mark Prince, Associate Professor and Director of My Mental Health Data Analysis and Dissemination, and 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. Responsibilities 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. Develop and manage program budgets in collaboration with the Principal Investigator, department, and school partners. Process procurement and reimbursements; facilitate vendor contracts and payments; reconcile accounts; and prepare financial reports. Serve 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; 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. 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. #J-18808-Ljbffr
$92k - $100k
...The University of Southern California is seeking a Clinical Project Manager to oversee NIH-funded research focused on behavioral health and mental health interventions. This hybrid role requires strong project management skills and a minimum of 5 years of relevant experience...Suggested$116.71k - $145.88k
...A leading healthcare company is seeking a Project Manager for Clinical Research to oversee the design and conduct of clinical trials in a remote setup. The successful candidate will ensure compliance with ethical standards, support study documentation, and lead a team...SuggestedRemote work$107k - $133k
...Job Summary The University of Southern California (USC) seeks a full‑time Clinical Operations Senior Project Manager for the USC+CHLA Alpha Clinic (AC). The AC is a pre‑clinical/clinical infrastructure program that supports the development, testing, and patient access...SuggestedFull timeTemporary work$29 - $33 per hour
...of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well... ...quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work...SuggestedHourly payFull timeWork at officeMonday to FridayShift workNight shift$35 - $40 per hour
...Clinical Research Coordinator – Los Angeles, CA (90033) Position Overview: This role is with a fast-paced clinical site experiencing significant... ...patient care and research integrity. Our ideal candidate will manage a significant portion of the studies, ensuring all aspects of...SuggestedMonday to Friday- ...reimagining men’s healthcare. Job Description The Clinical Research Coordinator will work under the... ..., Sub-Investigators, and/or Director/Manager of Clinical Research Operations to... ...overall direction of clinical research projects conducted on behalf of the sponsors at the...Local areaFlexible hours
- ...RDI is a trial management organization connecting IVD manufacturers and pharmaceutical companies with a network of doctors participating... ...provide sample procurement, conduct testing, and simplify the clinical trial process for our clients while recruiting, educating, and...
- ...ask for an accommodation or an alternative application process. Clinical Research Coordinator Beverly Hills, CA, US 5 days ago... ...the EMR (Electronic Medical Records) and CTMS (Clinical Trials Management System). Manage data collection and entry to eCRF (electronic...Temporary workLocal areaFlexible hours
$36.37 - $58.52 per hour
...Description The Department of Psychiatry is seeking to hire a Clinical Research Coordinator to join the TMS Research Service. You will contribute to the overall operational management of clinical research activities from design, set up, conduct, through closeout. Primary...$45k - $100k
...Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide At... ...coordinating study visits, collecting and managing data, and ensuring studies are conducted... ...‑on experience in lab courses, research projects, or clinical settings (internships, volunteering...Internship$25 - $40 per hour
...Part-time employment to start. This position is to fulfill a role for Clinical Research Coordinator at multiple sites (Oxnard, Palmdale, Valencia, Sherman Oaks, West Hills, Downtown LA, Inglewood). Some days you will work remote. Past experience as a Clinical Research...Hourly payPart timeLive inRemote work$75.71k - $129.79k
...Clinical Research Coordinator III Locations: Los Angeles, California Job Category: Professional Position Type: Full-Time Shift: Days Job... .... Develops procedures related to clinical trial coordination. Manages submission of regulatory documents in accordance with IRB, federal...Full timeWork experience placementLocal areaMonday to FridayShift work$71k - $80k
...Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West... ...trial and produced quality work. Job Duties Manage daily operations for assigned clinical trial projects Perform study procedures in accordance with GCP...Full time- ...Direct Jobs is seeking a Clinical Research Coordinator I in Los Angeles, CA. The role involves independently managing clinical research studies, ensuring compliance with federal regulations, and maintaining patient confidentiality. Responsibilities include coordinating...
- ...NRC Research Institute has been conducting clinical trials for the world’s pharmaceutical firms since 2004. We specialize in pharmaceutical... ...research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse...Full time
- ...Overview EXPERIENCED Clinical Research Coordinator - Onsite Job Details: 15-20 hours/week... ...team. The CRC will plan, coordinate, and manage all activities associated with the initiation... ...patient questionnaires. Update the project Clinical Trials Management system and the...Full timeWork at officeLocal areaRemote workVisa sponsorship
$70 - $78 per hour
...Clinical Trial Manager W2 Contract Pay Rate: $70 - $78 per hour Location: Remote Role - PST Job Summary: We are seeking an experienced and highly... ...across geographies Proficiency in Microsoft Word, Project, PowerPoint, Excel, and SharePoint Desired Skills and Experience...Hourly payContract workInterim roleRemote workFlexible hours$22 - $26 per hour
...Clinical Research Coordinator Pasadena, CA 91107 Overview Salary Range $22.00 - $26.00 Hourly Level Experienced Description... ..., assisting principal investigators in recruiting and management research studies directly affecting the eyecare industry. Essential...Hourly payWork at officeLocal area- ...Clinical Research Coordinator II The mission of the California Heart Center is to integrate quality health care, clinical research,... ...Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning,...Local areaImmediate startShift work
- ..., stores, evaluates, and distributes human specimens, which are maintained in association with the triad of accurate longitudinal clinical metadata, comprehensive genotype information, and serotypes. These resources are made available to research partners within IBIRI...Work at officeLocal area
$36.37 - $58.52 per hour
...and EEG operations (preferred) Analytical skills to evaluate clinical research protocols and regulatory requirements, identify... ..., email, and data entry systems Strong organizational skills with the ability to manage multiple projects and competing deadlines UCLA HealthHourly payRemote workMonday to Friday- ...A neurology practice in Los Angeles seeks a Clinical Research Coordinator II to manage various research studies, ensuring protocol compliance and data integrity. The role involves recruiting and documenting subjects while upholding standards of Good Clinical Practice....
- ...Come join our team! The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible...Full timeLocal area
$31 - $43 per hour
...environment, and endless growth opportunities. We are actively hiring Clinical Research Coordinators at our Century City site location. This... ...supplies). Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy. Perform...Work at officeLocal areaMonday to FridayShift workNight shift- ...A prominent healthcare research organization in Los Angeles is seeking an experienced Clinical Research Coordinator to manage clinical trials. This role involves coordinating activities, ensuring compliance with research protocols, and working closely with investigators...Full time
- ...Profound Research LLC is seeking a Clinical Research Coordinator I in Pasadena to support high-volume vaccine clinical trials. The role involves managing study activities, ensuring compliance with protocols, and leading patient interactions. The ideal candidate has relevant...Full timeContract work
- ...Profound Research Profound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research... ...Why this Role Exists The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with...
$6,892.14 - $11,089.02 per month
...the lives of people around the world. The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up... ...quality, compliant execution across complex research projects. Key Responsibilities Manage day-to-day operations...Live outFlexible hours- ...Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all... ...ready to step into real ownership of clinical trial coordination - managing your own studies, leading patient visits, and working with the...Work at office
- ...Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all... ...volume vaccine clinical trials at one of our sites. You'll help manage study activities, lead participant visits, complete protocol-...Full timeContract workFor contractorsWork at office
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