USC Rossier Global Executive Ed.D.
Clinical Operations Project Manager
USC Rossier Global Executive Ed.D., San Diego, California, United States, 92154
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Clinical Operations Project Manager
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USC Rossier Global Executive Ed.D.
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Clinical Operations Project Manager
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USC Rossier Global Executive Ed.D.
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Apply Keck School of Medicine San Diego, California
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.
Responsibilities
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
Serve as the primary point of contact and guidance expert for assigned studies
Provide work direction and delegate tasks to other staff personnel
Develop various study materials including protocol, training and procedures manuals, source documents, and work instruction documents
Develop 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 $85,008.75 - $105,954.56. 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 related field(s). Additional 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 diverse individuals and groups coordinating and executing study activities
Preferred Education Bachelor's degree and Master's degree in Neurosciences, Public Health, Pharmacology, or related fields.
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
Ability to handle several priorities within multiple, complex clinical trials
Strong understanding of current GCP guidelines
Proficient in OmniPlan or other timeline applications
Familiarity with academic medical centers
REQ20160121 Posted Date: 03/09/2025
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Clinical Operations Project Manager
role at
USC Rossier Global Executive Ed.D.
Ensure all your application information is up to date and in order before applying for this opportunity. 3 weeks ago Be among the first 25 applicants
Join to apply for the
Clinical Operations Project Manager
role at
USC Rossier Global Executive Ed.D.
Get AI-powered advice on this job and more exclusive features.
Apply Keck School of Medicine San Diego, California
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.
Responsibilities
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
Serve as the primary point of contact and guidance expert for assigned studies
Provide work direction and delegate tasks to other staff personnel
Develop various study materials including protocol, training and procedures manuals, source documents, and work instruction documents
Develop 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 $85,008.75 - $105,954.56. 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 related field(s). Additional 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 diverse individuals and groups coordinating and executing study activities
Preferred Education Bachelor's degree and Master's degree in Neurosciences, Public Health, Pharmacology, or related fields.
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
Ability to handle several priorities within multiple, complex clinical trials
Strong understanding of current GCP guidelines
Proficient in OmniPlan or other timeline applications
Familiarity with academic medical centers
REQ20160121 Posted Date: 03/09/2025
#J-18808-Ljbffr