Top 76 Clinical research associate Jobs in Ontario Ca

Clinical Research Specialist
Kelly Services —Irvine, CA
- $92,000 a year
- Full-time
- Nursing
- Bachelor of Science
- English
- Paid holidays
- Disability insurance
Quick Apply
Manager / Sr. Manager, Clinical Operations - FSP West Region
Thermo Fisher Scientific —California
- $115,000 - $178,000 a year
- Full-time
- Remote
- English
- Business development
- Travel
- Commuter assistance
- Paid parental leave
Clinical Research Associate I
City of Hope —Duarte, CA
- $33.80 - $43.22 an hour
- Full-time
- Clinic
- 1 year
- Associate's degree
Clinical Research Associate II
City of Hope —Duarte, CA
- $33.80 - $47.54 an hour
- Full-time
- Mid-level
- Clinic
- Associate's degree
3d
Clinical Research Coordinator I, Oncology
CHOC Children's —Orange, CA
- $29.48 - $48.61 an hour
- Full-time
- Microsoft Excel
- Writing skills
- Children
Clinical Research Assistant I
City of Hope —Duarte, CA
- $26.48 - $38.25 an hour
- Full-time
- Hospital
- Mentoring
- Associate's degree
3d
Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)
USC —Arcadia, CA
- $34.32 - $56.19 an hour
- 8 hour shift
- Word processing
- HIPAA
- Mid-level
Clinical Research Coordinator (San Francisco)
University of California, Riverside —Riverside, CA
- $34.37 - $55.27 an hour
- Full-time
- Spanish
- Psychiatry
- English
Clinical Trials Data Coord
City of Hope —Duarte, CA
- $30.67 - $47.54 an hour
- Full-time
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
Clinical Research Coordinator
University of California, Irvine —Orange, CA
- $37.56 - $61.91 an hour
- Weekends as needed
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)
Keck Medical Center of USC —Arcadia, CA
- $34.32 - $56.19 an hour
- 8 hour shift
- Background check
- Word processing
- HIPAA
Assoc Clinical Research Coord
City of Hope —Duarte, CA
- $27.88 - $43.22 an hour
- Full-time
- HIPAA
- Mid-level
- Office
Temporary Clinical Research Regulatory Coordinator
University of California, Irvine —Orange, CA
- $37.56 - $61.91 an hour
- Temporary
- Background check
- HIPAA
- English
- Paid holidays
- Health insurance
Research Data Coordinator - Hybrid
University of California, Irvine —Orange, CA
- $37.56 - $61.91 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Clinical Research Recruitment Coordinator
Irvine Clinical Research —Riverside, CA
- $25 an hour
- Full-time
- Hybrid work
- Public speaking
- Clinic
- Older adults
- Dental insurance
- Paid time off
Quick Apply
Research Associate
Heluna Health —Santa Ana, CA
- $28.82 - $36.25 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
Research Assistant
Flourish Research —Covina, CA
- $25 - $30 a year
- Full-time
- Vital signs
- Computer literacy
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Clinical Study Coord
City of Hope —Irvine, CA
- $44.90 - $69.60 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
12d
Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)
USC Arcadia Hospital —Arcadia, CA
- $34.32 - $56.19 an hour
- 8 hour shift
- Background check
- Word processing
- HIPAA
Assistant Regulatory Affairs Coordinator - Hybrid
University of California, Irvine —Orange, CA
- $31.11 - $51.25 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan

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Clinical Research Specialist

Kelly Services -
Irvine, CA

Quick Apply

Job Details

Full-time
$92,000 a year

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Vision insurance
Retirement plan
Paid sick time

Qualifications

Technical writing for researchers
Content creation for technical audiences
Regulatory compliance
English
Legal compliance
Standard operating procedures (SOPs)
Stakeholder management

Full Job Description

Clinical Research Specialist
Hybrid - onsite every Monday, Wednesday, and every other Friday
Pay Rate: 92,000

Clinical Research Specialist Requisition

Job Overview

This Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.

Duties & Responsibilities

Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate procedures and guidelines, this position:

Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, under supervision;
Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures;
May serve as the primary contact for clinical trial sites (e.g. site management);
Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports);
Supports applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed;
Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials;
Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel;
Interfaces and collaborates with Clinical Research Associates (CRAs);
Assists in overseeing and supports the development and execution of Investigator agreements and trial payments;
Assists in clinical data review to prepare data for statistical analyses and publications;
May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need;
May provide on-site procedural protocol compliance and data collection support to the clinical trial sites;
Assists in tracking assigned project budgets;
May perform other duties assigned as needed;
Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders;
Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures;
Should develop a strong understanding of the pipeline, product portfolio and business needs;
Generally manages work with supervision. Independent decision-making for simple situations but requires guidance for complex situations.

Experience and Education

Education

Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

Experience

BS with at least 2 years, MS and PhD with at least 1 year of relevant experience preferred.
Previous experience in clinical research or equivalent is desired.
Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,…).
Clinical/medical background is a plus.
Medical device experience is a plus.

Required Knowledge, Skills, Abilities, Certifications/Licenses and Affiliations

Functional and Technical Competencies:

Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations;
Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations;
Presentation and technical writing skills;
Written and oral English communication skills.

Leadership Competencies:

Leadership required in alignment with Company Leadership Imperatives:

Connect - Develop collaborative relationships with key internal and external stakeholders.
Shape - Actively participate in departmental process improvement activities.
Lead - Take ownership in critical scientific thinking and development of self and engage in transparent and constructive conversations.
Deliver - Strive to ensure all deliverables on allocated studies are met on time, within budget and in compliance to SOPs and regulations.

Location & Travel Requirements
Primary location for this position is Irvine, CA. At management discretion, the position may be performed remotely.
Ability to travel approximately 20% depending on the phase of the program.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

Quick Apply

Refine Your Search

clinical research associate jobs in ontario ca

Clinical Research Specialist

Manager / Sr. Manager, Clinical Operations - FSP West Region

Clinical Research Associate I

Clinical Research Associate II

Clinical Research Coordinator I, Oncology

Clinical Research Assistant I

Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)

Clinical Research Coordinator (San Francisco)

Clinical Trials Data Coord

Clinical Research Coordinator

Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)

Assoc Clinical Research Coord

Temporary Clinical Research Regulatory Coordinator

Research Data Coordinator - Hybrid

Clinical Research Recruitment Coordinator

Research Associate

Research Assistant

Clinical Study Coord

Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)

Assistant Regulatory Affairs Coordinator - Hybrid

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Clinical Research Specialist Requisition

Job Overview

Duties & Responsibilities

Experience and Education

Education

Experience

Required Knowledge, Skills, Abilities, Certifications/Licenses and Affiliations

Functional and Technical Competencies:

Leadership Competencies:

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