Houston, Texas
Saint Louis, Missouri
Miami, Florida
Miami, Florida
Posted: 15-Feb-25
Location: Los Angeles, California
Categories:
Internal Number: 146272209
The Assistant Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the coordination of research activities for one or more studies. The incumbent recognizes and performs necessary tasks to coordinate projects and prioritizes work to meet necessary deadlines. The incumbent participates in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Study Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. The responsibilities outlined in the job description provide a general overview of duties and tasks performed by Clinical Research Coordinators.
Performance of duties and tasks will vary based on the department operations, the type of study and scope of service.
All Required
Minimum of 1+ years of experience in a clinical research setting
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 effectively communicate to and interact with patients in a compassionate and kind
manner.
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.
Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.
Organization skills to create and maintain administrative and regulatory files effectively as well
as independently balance the various tasks to ensure deadlines are met.
Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform
daily tasks efficiently and accurately.
A learning and professional growth mentality so that new software tools, systems, and processes
can be adopted quickly and efficiently.
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.
Strong verbal and written communication skills to effectively establish rapport, building
collaborative relationships, and communicate complex concepts and ideas in an easy-tounderstand
manner.
Ability to adapt to changing job demands and priorities, remain flexible including working
flexible hours to accommodate research deadlines.
Ability to handle confidential information with judgement and discretion. All Required
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…
Preferred
Bachelor’s degree
