Atlanta, Georgia
Kula, Hawaii
Washington,
Posted: 29-Jan-26
Location: Los Angeles, California
Categories:
Internal Number: 150832519
The Data Coordinator plays a key role in managing the operational aspects of clinical research studies throughout their lifecycle-from design and initiation to conduct and closeout. In this position, you will oversee the implementation of research activities for one or more studies, ensuring tasks are prioritized and completed within required timelines. Responsibilities include planning and organizing activities to maintain strict adherence to study protocols and applicable regulations, including institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP) standards. Work collaboratively with the Principal Investigator (PI), ancillary departments, central research teams, sponsors, and other stakeholders to support all facets of study administration. This includes ensuring compliant study conduct, managing financial aspects, and coordinating adequate personnel resources.
The full hourly salary range for this position is $35.31 - $56.82.
Required:
· Bachelor's degree in related area and/or equivalent combination of education and experience.
· Minimally 2+ years of previous study coordination or clinical research coordination experience
· Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.
· Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.
· Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
· Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.
· Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
· Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
· High degree of concentration and focus in a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual
· Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc.
