Clinical Research Coordinator - Surgery

University of California - Los Angeles Health; Los Angeles (CA); On-site; USD 52,000 - 84,000; Full time

Job summary

University of California - Los Angeles Health is seeking an experienced Clinical Research Coordinator to support interventional trials across multiple divisions. You will coordinate and manage study activities for drug and device trials, including participant recruitment, study implementation, data collection, and regulatory compliance.

Responsibilities include coordinating budgets, ensuring adherence to FDA CFR and ICH GCP guidelines, and collaborating with teams to meet deadlines while

Qualifications

• Bachelor's Degree or 1-3 years of prior study coordination or clinical research coordination experience.
• Strong verbal and written communication and interpersonal skills.
• Solid organizational skills to manage multiple projects and deadlines.
• Analytical abilities to identify problems and determine solutions.
• Ability to adapt to changing demands and work flexible hours for deadlines.
• Professional response to situations and discretion with confidential information.
• Working knowledge of clinical research regulatory framework and institutional requirements.
• Familiarity with FDA CFR and ICH GCP guidelines.

Responsibilities

• Coordinate and manage interventional clinical trials across divisions.
• Recruit participants and oversee study implementation and data collection.
• Ensure compliance with regulatory requirements and study protocols.
• Prepare budgets and support budgeting processes for trials.

Skills

Verbal communication

Written communication

Interpersonal skills

Organizational skills

Analytical skills

Adaptability

Time management

Data entry

Confidentiality

Education

Bachelor's degree

Job description

Description

The Department of
Surgery is seeking an experienced Clinical Research Coordinator to supportinterventional
clinical trials across multiple divisions. This role will be responsible for
coordinatingand
managing study activities for both drug and device trials, including
participant recruitment, studyimplementation,
data collection, and ensuring compliance with all regulatory requirements,institutional
policies, and study protocols.

Hourly
salary range: 38.19 - 61.45.

Qualifications

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.