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Description

The Clinical Research Coordinator (CRC) 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

implementation of research activities for one or more studies. The CRC

recognizes and performs necessary tasks to manage projects and prioritizes work

to meet necessary deadlines. The CRC is 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). The CRC 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.

Pay Range: $32.65 - $52.53 Hourly

Qualifications

Required:

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.

Available to work in more than one environment, travel to

meetings, off-site visits, conferences, etc.

Preferred:

Bachelor's Degree or 1-3 years of previous study coordination or clinical

research coordination experience

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.