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Description

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. Recognize

and perform necessary project management tasks and prioritizes 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.

Salary

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.

+ Advance 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.