New 
Clinical Operations Project Manager
 University of Southern California | |
 United States, California, San Diego | |
 Nov 05, 2026 | |
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Collaborates with Project Director and other functional groups to develop clinical trial scopes of work and objectives. Assesses feasibility of clinical projects, identifies project priorities, enforces project timelines, and ensures that milestones are met. Operationalizes, implements and manages clinical trial protocols at multiple study sites. Develops written materials to guide study sites in clinical trial execution. Collaborates with other functional groups to create, revise, implement and monitor standard operating procedures (SOP) and internal procedural guidelines. Serves as point of contact and guidance expert for assigned projects and studies. Organizes and executes training for site principal investigators and study staff.
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. Job ID REQ20182698
Posted Date 11/04/2026 Apply
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