Logistics Analyst- SOM: Clinical and Translational Science Center - Sacramento Campus
The Clinical and Translational Science Center (CTSC) serves as a catalyst to support biomedical research projects by providing services and resources to investigators, staff, scholars and trainees, and community.
Job Summary Final Filing Date : 08/03/2021 Salary Range : $23.66 to $47.51 (salary grade 20) Salary Frequency : Hourly Appointment Type : Career Percentage of Time : 100% Shift Hour : 8:30am to 5:00pm (30 minute lunch) Location : CTSC Building City : Sacramento Union Representation : No Benefits Eligible : Yes
We offer exceptional employment benefits including medical, dental, and vision plans, generous paid vacations and holidays, excellent retirement savings and investment plans, continuing education, and reduced fee and scholarship programs.
THIS IS NOT AN H1- B OPPORTUNITY
Responsibilities This position serves as a Logistics Analyst for the CTSC Clinical Trials Office (CTO) Regulatory Team at the UC Davis School of Medicine. The position reports to the Regulatory Supervisor, Clinical Trials Office, and require frequent interaction with the various research related functional offices and programs such as the IRB and Contracts. Key functions of this position are to support the CTSC mission, specifically, logistical implementation of the start-up phase of clinical trials, feasibility assessment of new grant proposals, education and training for UC Davis investigators and clinical research staff on start up processes.
Under general supervision, this position is responsible to support the Logistics team in the CTSC Clinical Trials Office, set and meet milestones and deliverables, and provide creative solutions to fulfill programmatic needs. Specific duties include but not limited to: providing hands-on support to clinical trials during the start-up and transitional phases, as well as providing consultations, offering expert opinions, participating in improvement of feasibility and start up processes. This individual will work on problems of diverse scope and complexity in close alignment with the IRB administration, Health Contracts, Health Compliance Office, as well as other CTSC teams.
Minimum seven years professional clinical research administration and regulatory compliance experience in a health care or academic setting. Demonstrated experience in study management, start-up and implementation.
Advanced background and knowledge of clinical trial operations, including but not limited to IRB and FDA requirements. Clinical research certification (SOCRA or ACRP) is desired. Clinical Research Experience at UCD Health is strongly preferred.
Possess working knowledge of federal & state regulations, GCP guidelines, HIPAA, institutional policies, and SOPs for conduct of human subjects research in an academic environment.
Administrative skills and ability to exercise good judgment, initiative, and resourcefulness, and to use these skills when managing staff and workload.
Possess good investigative skills with a high degree of accuracy and attention to detail.
Possess good presentation skills for education and training programs geared toward university research faculty, research staff, in all research departments, divisions, and for CTSC staff and administrators
Analytical skills to evaluate information, practices, and procedures, formulate logical and objective conclusions, and make recommendations for effective solutions, strategies, and/or approaches.
Ability to organize and analyze data in complex spreadsheets under general supervision.
Knowledge and experience working with key administrative software and computer systems including Windows or Mac OS, Microsoft Office Suite, web browser applications, email applications, and Access databases.
Combination of working off site and on site depending on the business needs. Travel is required (15%). This position may be subject to a criminal background investigation, drug screen, Live Scan fingerprinting, medical evaluation clearance, and functional capacity assessment.
EEO The University of California is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.
The University of California is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.
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UC Davis is the home of the Aggies — go-getters, change makers and problem solvers who make their mark at one of the top public universities in the United States. Since we first opened in 1908, we’ve been known for standout academics, sustainability and Aggie Pride as well as valuing the Northern California lifestyle. These themes are woven into our 100-plus-year history and our reputation for solving problems related to food, health, the environment and society.Our 5,300-acre campus is in the city of Davis, a vibrant college town of about 68,000 located in Yolo County. The state capital is 20 minutes away, and world-class destinations such as the San Francisco Bay Area, Lake Tahoe and the Napa Valley are within a two-hour drive.