- Assisting with the procurement and distribution of supplies and other materials necessary for the successful conduct of the trial
- Utilizing and maintaining spreadsheets and other systems to track and disseminate information necessary for the effective oversight of clinical trial sites and study activities
- Drafting communications and advising clinical trial sites in a manner consistent with study procedures and ICH-GCP (Good Clinical Practices) guidelines
- Drafting, facilitating the review of, and distributing study materials such as source documents, procedures manuals, training certificates, etc.
- Organizing and filing essential documents consistent with the study protocol's Trial Master File
- Facilitating teleconferences, meetings and training sessions The ideal candidate will have strong organizational capabilities, excellent written and oral communications skills, and demonstrated ability to support clinical trials or similar research activities. Two years of experience is preferred. Location: San Diego, CA The hourly rate range for this position is $ $31.77. 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.
Minimum Education: High school or equivalent Minimum Experience: 1 year Minimum Field of Expertise: Knowledge of data collection procedures and some experience with proposal preparation and production of technical documents -
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Clinical Trials Project Assistant - San Diego, CA, United States - Keck School of Medicine
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 dependable and detail-oriented Project Assistant to support the ATRI Clinical Operations team specifically with the daily processing of supply management and in addition, managing the implementation, maintenance and closeout of Alzheimer's disease clinical trials at multiple national and international ATRI clinical trial study sites.
The ATRI Project Assistant serves a key support role on the Clinical Operations team. Responsibilities of the Project Assistant position include, but are not limited to: