UCLA Health Senior Clinical Research Coordinator - Los Angeles, California
The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout.
The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and / or programmatic clinical research activities.
Ready to apply Before you do, make sure to read all the details pertaining to this job in the description below.
Recognize and perform necessary project management tasks and prioritize work to reach scheduled goals. The Senior Clinical Research Coordinator is a technical leader responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner.
This position may supervise and train others on projects as necessary. Work with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of the compliance, financial, personnel, and other related aspects of studies.
Offers are determined based on various factors including, but not limited to, qualifications, experience, and equity. The full annual salary range for this position is : $82,713.61 - $133,060.10.
Qualifications
Required :
- Bachelor's Degree or three to seven years of study coordination or clinical research coordination experience
- Analytical skills sufficient to work and solve problems
- Ability to work flexible hours to accommodate research deadlines
- Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines
- Ability to be flexible in handling work delegated by more than one individual or in the course of delegating work
- Skill in managing diverse, complex tasks and information transfer among multiple constituents
- Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets
- Advanced knowledge of the clinical research regulatory framework and institutional requirements
- Ability to supervise and delegate clerical work as needed
- Advanced knowledge of Good Clinical Practice (GCP) for clinical research
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.
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