Clinical Research Coordinator

4 weeks ago


Los Angeles, United States UCLA Health Full time

General Information

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Work Location: Los Angeles, USA

Onsite or Remote

Flexible Hybrid

Work Schedule

Monday - Friday 8am - 5pm (hours may vary)

Posted Date

03/12/2024

Salary Range: $32.65 - 52.53 Hourly

Employment Type

2 - Staff: Career

Duration

indefinite

Job #

14685

Primary Duties and Responsibilities

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The Department of Surgery is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities of multiple studies. From design, set up, conduct, through closeout, you will be responsible for the implementation of research activities including the following:

* Recognizing and performing necessary tasks to manage projects and prioritizes work to meet necessary deadlines.
* Be responsible for 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).
* Collaborating with the Principal Investigators (PIs), 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.

Pay Range: $32.65 - $52.53 hourly

Job Qualifications

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Required:

Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.

Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.

Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.

Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.

Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.

Ability to respond to situations in an appropriate and professional manner.

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.

Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.

Ability to handle confidential material information with judgement and discretion.

Working knowledge of the clinical research regulatory framework and institutional requirements.

Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.

Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.

Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.



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