Clinical Operations Project Manager

University of Southern California

San Diego (CA)

On-site

USD 89,000 - 118,000

Full time

35 hours ago
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Job summary

The University of Southern California (ATRI) in San Diego seeks a Project Manager to oversee ATRI clinical trials across multiple sites, ensuring timely, compliant study execution. You will collaborate with the Project Director and cross-functional teams to plan, implement, monitor, and closeout trials, while developing essential study materials and ensuring quality deliverables.

The ideal candidate has 2–3 years of clinical trials experience and strong interpersonal, written, and organizational

Qualifications

  • Bachelor's degree in Biological Science or related field required.
  • Experience in clinical trials and on-site monitoring preferred.
  • Familiarity with ICH-GCP guidelines and FDA guidance documents.
  • Excellent written and verbal communication; strong organizational skills.

Responsibilities

  • Coordinate planning and administration of multi-site clinical trials.
  • Set and maintain priorities and timelines for studies across multiple sites.
  • Lead study planning meetings, manage minutes and action-item tracking.
  • Serve as primary contact and guidance for assigned studies.
  • Provide work direction and delegate tasks to staff.
  • Develop study materials: protocols, training manuals, source documents.
  • Create templates and guidelines per SOPs and regulations.

Skills

Clinical trials
Medical devices knowledge
Policy & compliance
Technical documentation
Data management
Project leadership
Communication skills

Education

Bachelor's degree in Biological Science or related field
Master's degree in Neurosciences or Public Health or Pharmacology or related field

Tools

OmniPlan
Microsoft Office

Job description

The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute comprised of an expert panel of scientific collaborators, committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.

The ATRI is seeking a motivated, dependable, and experienced Project Manager to support ATRI clinical research efforts.

The Project Manager is a highly visible role responsible for managing the successful execution of ATRI clinical trials.

Responsibilities include, but are not limited to:

  • Collaborate with the Project Director and other functional groups in the planning and administration of all phases of multi-site clinical trials
  • Set and maintain priorities and timelines for project implementation, maintenance, and closeout of clinical trials across multiple national and international ATRI clinical trial study sites
  • Conduct and drive study planning meetings including the management of meeting minutes, logging action items and decisions, and tracking action items to completion
  • Serves as the primary point of contact and guidance expert for assigned studies
  • Provides work direction and delegates tasks to other staff personnel
  • Development of various study materials including protocol, training and procedures manuals, source documents, and work instruction documents
  • Development of templates and guidelines, informed by regulations, policies, and standard operating procedures (SOPs) for the management of assigned studies, as well as departmental initiatives aimed at improving process and efficiency

The ideal candidate will have excellent interpersonal skills for communicating with all levels of personnel and groups and demonstrated ability to successfully operationalize and manage all clinical trial components. Two to three years of experience in clinical trials is required.

Location: San Diego, CA

The annual base salary range for this position is $88,721.66 - $118,129.88.

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 degree In Biological Science Or in related field(s) Addtional Education Requirements Combined experience/education as substitute for minimum education

Minimum Experience: 2 years in on-site clinical trial monitoring.

Minimum Skills: Industry experience in a pharmaceutical, biotechnology, clinical research organization and/or nursing setting Demonstrated experience using medical devices and terminology. Experience applying policies and procedures, with some familiarity with ICH-GCP guidelines and working knowledge of FDA guidance documents. Skilled at technical documentation and writing, and at assembling, organizing and conceptualizing numerical data in spreadsheets, databases, reports and presentations. Lead/guidance skills, with the ability to manage and prioritize different tasks and projects. Deft interpersonal skills for communicating with all levels of staff and various individuals and groups coordinating and executing study activities.

Preferred Education: Bachelor's degree And Master's degree In Neurosciences Or Public Health Or Pharmacology Or in related field(s)

Preferred Certifications: Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC).

Preferred Experience: 4 years

Preferred Skills: Experience in data management. Excellent written and verbal communication skills to express complex ideas to study staff at research and clinical institutions. Ability to handle several priorities within multiple, complex clinical trials. Strong understanding of current GCP guidelines applicable to the clinical research conduct. Proficient in OmniPlan or other timeline applications. Familiarity with academic medical centers.

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 (213) 821-8100, or by email at uschr@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

USC is a leading private research university located in the heart of downtown Los Angeles – a global center for arts, technology and international business. As the largest private employer in the city – responsible for more than $5 billion annually in economic activity in the region – we offer the opportunity to work in a dynamic and diverse environment, in careers that span a broad spectrum of talents and skills. As a USC employee, you will enjoy excellent benefits and perks, and you will be a member of the Trojan Family - the faculty, staff, students and alumni who make USC a great place to work.

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