Clinical Operations Project Manager
Clinical Operations Project Manager
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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 Alzheimers 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 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 multisite 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 $85008.75 $105954.56. 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 candidates 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: Bachelors degree In Biological Science Or in related field(s)Additional Education Requirements: Combined experience/education as substitute for minimum education
Minimum Experience: 2 years in onsite 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 ICHGCP 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: Bachelors degree And Masters 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 theBackground Screening Policy Appendix Dfor 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 ator by email at. Inquiries will be treated as confidential to the extent permitted by law.
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Experience:IC
Employment Type
Full-Time
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