Clinical Project Manager
$92k - $100kUniversity of Southern California
Clinical Project ManagerThe 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 QualificationsBachelor's degree or combined experience/education as substitute for minimum educationMinimum 5 years of relevant experience in clinical research coordination, project management, or related workPreferred QualificationsMaster's degree7 or more years of relevant experience in academic or clinical research environmentsExperience managing complex, multi-component research projects and interdisciplinary teamsRequired SkillsStrong analytical, problem-solving, and organizational skillsExcellent verbal and written communication skillsDemonstrated ability to manage multiple priorities, meet deadlines, and work independentlyStrong interpersonal skills with a customer service-oriented mindsetAbility to work collaboratively with investigators, staff, and institutional partnersFamiliarity with research compliance, quality assurance, and data management processesAbility 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 LocationThis 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.CompensationThe 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.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 the Background Screening Policy Appendix D for 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 View phone number on click.appcast.io, or by email at View email address on click.appcast.io . Inquiries will be treated as confidential to the extent permitted by law.
$31.51 - $62.64 per hour
...Description The Project Manager (PM) for the Division of Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIOUS Network. Under the direction of the CTD Manager, investigators, and Senior Management, the PM contributes to protocol...SuggestedHourly payLocal areaShift work- 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...Suggested
$31.51 - $62.64 per hour
...Description The Project Manager (PM) for the Division of Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIO-US Network. Under the direction of the CTD Manager, investigators, and Senior Management, the PM contributes to...SuggestedHourly payFull timeShift work- ...diabetes, touching thousands of lives daily. The Opportunity focuses on managing clinical studies, guiding strategy with R&D, Regulatory Affairs, Sales and Marketing, and mentoring junior project managers to ensure on-time, within-budget delivery. #J-18808-Ljbffr AbbottSuggested
- DescriptionJob Summary: Collects data for clinical trials research, independently. Prepares... ...feedback to research staff and management. Supports and develops materials for the... ...internally funded standard and non-standard projects. Drafts and/or prepares and submits clinical...SuggestedFor contractorsFor subcontractorLocal area
$120k - $135k
...Clinical Project Manager - Oncology (Client Dedicated/Remote) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes...Contract workWork at officeRemote workWorldwideFlexible hours$90k - $180k
...routine fingersticks. The Opportunity Will be required to manage at least one primary project; Depending on scope and phase of project, may support... ...expertise throughout the development and implementation of clinical studies. Interacts with various study support groups and...Work experience placementLocal area- ...Job TitleClinical Research Coordinator IIJob DescriptionThe Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating...Local area
- ...related area and/or equivalent combination of education and experience. (Required)Minimally 2+ years of previous study coordination or clinical research coordination experience. (Required)Interpersonal skills to effectively communicate information in a timely, professional...Local areaRemote workMonday to FridayFlexible hours
- ...Clinical Research CoordinatorWe are seeking a dedicated Clinical Research Coordinator to join our team in Inglewood, California. In this... ...guidelines. This position involves screening participants, managing study documentation, and supporting study procedures to ensure...Contract workWork at office
- ...Innovo Research is seeking a Senior Clinical Research Coordinator to coordinate daily operations for studies at our partner site. You will supervise staff, ensure protocol compliance, and support regulatory submissions while maintaining high quality data and subject safety...
$93.93k - $151.1k
...Description The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up... ...activities. Recognize and perform necessary project management tasks and prioritizes work to...Local areaFlexible hours- ...MUST BE W2 EMPLOYEES OF THE SUBMITTING AGENCY*** Senior Clinical Research Coordinator Location: 10920 Wilshire Blvd, Los... ...and sponsor interactions. Additional Information • Budget management experience is not required. • NIH and multicenter trial experience...
$120k - $150k
...record of completing large scale structures, paving and utlitlies projects across teh state of NJ. We are looking to add to our team. If... ...Job Details Job Details Are you an experienced Project Manager with a background in civil construction? Do you have a passion...Permanent employmentFor contractorsFor subcontractorLocal area- ...Clinical Research Coordinator IIThe Clinical Research Coordinator II is a critical, high-autonomy role that makes clinical research accessible... ...the Principal Investigator (PI), this individual independently manages the full study lifecycle—from feasibility and start-up, through...Work at officeFlexible hoursNight shift
$62.4k - $83.2k
...Clinical Research Coordinator Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind on... ...patient safety, and operational excellence. Job Duties Study Management: Serve as the primary or co-coordinator for assigned Phase II/...Hourly payFull time$27 per hour
...Clinical Research Coordinator I Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and...Full time- National Clinical Trials Inc. is seeking a detail-oriented Clinical Research Coordinator II (CRC II) to join our team in Los Angeles, CA. You will coordinate and manage clinical trials, ensuring FDA/GCP/ICH compliance, and serve as the main liaison with sponsors and IRB...
$24 - $39.76 per hour
A leading medical center in Los Angeles seeks a Clinical Research Coordinator I to manage patient scheduling, document research activities, and comply with federal regulations. Ideal candidates have a high school diploma or GED, with a preference for a bachelor's degree...Hourly payFull time- Irvine Clinical Research - West Los Angeles / Inglewood location seeks a Clinical Research Coordinator I to manage day-to-day trial operations, coordinate visits, and ensure data integrity under GCP standards. You will work closely with Principal Investigators and our clinical...Full time
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator to support clinical research protocols effectively. This role involves processing laboratory specimens, maintaining records, and facilitating patient recruitment. The ideal candidate holds a High School...Remote work
- A leading medical center in Los Angeles is seeking a Clinical Research Coordinator II to manage study coordination, including patient scheduling and data collection. The role requires effective communication with medical personnel and compliance with FDA regulations. Candidates...
- CenExel Clinical Research in Los Angeles is hiring a Clinical Research Coordinator to support coordination of clinical trials in line with ICH, GCP, and study guidelines. The role involves data collection, regulatory duties, and quality control across multiple sites. The...Full time
$28 - $30 per hour
Description Clinical Research Coordinator Kelly® Science & Clinical is seeking a Clinical Research Coordinator for a 5-month temporary... ...studies by screening and enrolling participants, collecting and managing data, supporting study visits and procedures, maintaining...Temporary workLocal areaMonday to Friday- UCLA Health is seeking a Clinical Research Coordinator to join a centralized clinical research team focusing on pediatric trials. This... ...encompasses various activities including recruitment, data management, and adherence to clinical research standards. The ideal candidate...Flexible hours
$65.52k - $87.36k
...tomorrows for the children and families we serve. Overview Schedule: Monday-Friday Purpose Statement/Position Summary: The Clinical Research Coordinator I assists Principal Investigators and other study team members in the coordination and conduct of clinical...Full timeWork experience placementLocal areaMonday to Friday- UCLA Health in Los Angeles, CA is seeking an experienced Clinical Research Coordinator to support interventional clinical trials in the Department of Surgery. You will coordinate and manage activities for drug and device trials, including participant recruitment, study...
- 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... ...explaining patient questionnaires. Update the project Clinical Trials Management system and the...Full timeWork at officeLocal areaRemote workVisa sponsorship
$38.19 - $61.45 per hour
UCLA Health in Los Angeles is seeking an experienced Clinical Research Coordinator to support interventional clinical trials across multiple divisions within the Department of Surgery. You will coordinate study activities, oversee recruitment, data collection, and ensure...Hourly pay- Cedars-Sinai Medical Center in Los Angeles is seeking a Clinical Research Coordinator II to support the Pancreatic Research Program. This role involves coordinating research activities, ensuring compliance with regulations, and enhancing patient enrollment in clinical...
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