Top 28 Investigator assistant Jobs in Orange County Ca

ASST. RESEARCH DATA COORDINATOR - HYBRID
University of California, Irvine —Orange, CA
- $27.40 - $45.13 an hour
- Full-time
- Remote
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Investigative Assistant I/II
City of Cypress, CA —Cypress, CA
- $21.90 - $27.90 an hour
- Clean driving record
- Mid-level
- High school diploma or GED
Asset Protection Investigator
Neiman Marcus —Newport Beach, CA
- $22.61 - $28.26 an hour
- Full-time
- Computer literacy
- Writing skills
- Conflict management
- Disability insurance
- Health insurance
Asst. Clinical Research Coordinator - Hybrid
University of California, Irvine —Orange, CA
- $29.63 - $48.81 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Regulatory Affairs Coordinator
University of California, Irvine —Orange, CA
- $35.77 - $58.96 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Research Assistant II
Helios Clinical Research —Cerritos, CA
- Full-time
- Vital signs
- Bachelor's degree
- No travel
Quick Apply
Dental Assistant II - Correctional Health Services
County of Orange —Santa Ana, CA
- $22.18 - $29.45 an hour
- Weekends as needed
- Background check
- Microsoft Outlook
- Computer literacy
- Health insurance
Physician Assistant
Altasciences —Cypress, CA
- On call
- Paid holidays
- Health insurance
Clinical Research Site Manager
Knowledge Research Center —Orange, CA
- $110,000 - $120,000 a year
- Full-time
- Background check
- Pass drug screening
- US work authorization
Clinical Research Assistant
Mariposa Medical, LLC —Long Beach, CA
- $23 - $25 an hour
- Full-time
- Mid-level
- In-person
- Health insurance
- Dental insurance
Quick Apply
Regulatory Affairs & Quality Assurance Manager
University of California, Irvine —Orange, CA
- $97,000 - $182,200 a year
- Weekends as needed
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Beall Applied Innovation Assistant Director, Licensing
University of California, Irvine —Irvine, CA
- $132,600 - $259,800 a year
- Contract
- Background check
- 3 years
- Supervising experience
- Health insurance
- Retirement plan
Sub-Investigator (NP or PA) - Westside Los Angeles
Irvine Clinical Research —Long Beach, CA
- $125,000 - $140,000 a year
- Full-time
- Management
- Psychiatry
- English
- Dental insurance
- Paid time off
Quick Apply
Health Services Manager, Senior
County of Orange —Santa Ana, CA
- $67.63 - $93.67 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance
Clinical Research Manager
University of California, Irvine —Orange, CA
- $97,000 - $182,200 a year
- Overtime
- Background check
- 7 years
- Microsoft Excel
- Health insurance
- Retirement plan
Psychiatrist - CHS
County of Orange —Santa Ana, CA
- $320,923.20 - $348,150.40 a year
- Weekends as needed
- Bilingual
- Background check
- Psychiatry
- Paid holidays
- Health insurance
7d
Post-Doctoral Research Scientist – RNA Analysis
Zymo Research Corporation —Irvine, CA
- $85,000 - $100,000 a year
- Email
- Business development experience
- Doctor of Philosophy
- Senior level
- Paid holidays
- Health insurance
Quick Apply
18h
Post-Doctoral Research Scientist - RNA Analysis
Zymo Research —Irvine, CA
- $85,000 - $100,000 a year
- Email
- Business development experience
- Doctor of Philosophy
- Senior level
- Paid holidays
- Health insurance
1d
Director of Psychiatric Mental Health Nurse Practitioner Program
Western University of Health Sciences —Pomona, CA
- $125,000 - $133,250 a year
- Full-time
- Background check
- Nursing
- Doctoral degree
- Paid time off
- Retirement plan
Clinical Research Coordinator Manager - Oncology
Helios Clinical Research —Cerritos, CA
- $80,000 - $87,000 a year
- Full-time
- HIPAA
- Clinic
- Ability to lift 50 pounds
Quick Apply

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ASST. RESEARCH DATA COORDINATOR - HYBRID

University of California, Irvine -
Orange, CA

Apply Now

Job Details

Full-time
$27.40 - $45.13 an hour

Benefits

Health insurance
Retirement plan

Qualifications

Records maintenance
Informed consent
Filing
Research report preparation
Informed consent procedures implementation
Clinical data report preparation
Data interpretation
Research administration
Communication with regulatory authorities for clinical trials
IRB compliance
Clinical trial support in drug product development
Clinical consent forms
Ethical review application preparation
Pharmaceutical research experience
Medical terminology

Full Job Description

Overview:

Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation’s top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It’s located in one of the world’s safest and most economically vibrant communities and is Orange County’s second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide.

To learn more about UC Irvine, visit www.uci.edu.

The NCI-designated Chao Family Comprehensive Cancer Center (CFCCC) is a campus-wide multidisciplinary matrix organization whose goal is to promote and enhance cancer-relevant research and patient care at UC Irvine. The CFCCC provides research resources to its ~175 members engaged in research and offers multidisciplinary cancer care to its patients.

Responsibilities:

Under supervision of the Clinical Research Manager, the Assistant Research Data Coordinator (ARDC) supports the clinical research efforts of the CFCCC by providing comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols according to Good Clinical Practices (GCP),
internal standard operating procedure (SOPs), and University policies and procedures.

The incumbent is responsible for the timely and accurate collection and coordination of data submission to study sponsors ensuring quality control and leading to timely milestone payments. This includes responsibility for the compilation and transcription of research patient data and study-related
information into case report forms (CRFs) into sponsor specific electronic data capture systems (EDC).

S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of cancer-related trials.

Serve as the liaison to sponsors, governing agencies and facilitate transmission of verbal and written communication to national cooperative oncology groups, pharmaceutical companies and other research
entities as needed.

The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and
Drug Administration (FDA), and sponsor monitors.

In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI).

Qualifications:

Required:

Demonstrated problem solving capabilities to resolve concerns that arise unexpectedly
Ability to independently exercise discretion and sound judgment
Ability to take initiative and demonstrate strong commitment to duties
Access to transportation to off-site research locations
Demonstrated high-level communication skills to convey information in a clear and concise way, synthesizing information and presenting it to others
Demonstrated ability to research, properly evaluate information, and prepare concise, well organized reports, summaries, and correspondence
Ability to interact with the public, faculty, and staff
Willingness to work as a supportive, cooperative member of an interdisciplinary team
Ability to work collegially and cooperatively in a small office and to establish and maintain cooperative working relationships
Demonstrated skill in interacting with persons of various social, cultural, economic and educational backgrounds
Ability to work both independently and as part of team
Demonstrated track record of human subject's research (Phase I, II, III drug trials, and device trials) coordination, informed consent procedures and documents, and IRB submissions.
Foster and promote a positive attitude and professional appearance
Ability to establish and maintain files and records
Working knowledge of computer software including Microsoft Office (Outlook, Word, Excel, and PowerPoint
Ability to think critically, compiles data from various sources, analyze data, and prepare reports.
Ability to analyze problems, implement solutions and multitask
Strong attention to detail
Working knowledge of medical terminology and accurately read progress notes in patient charts
High level of integrity and honesty in maintaining confidentiality
Demonstrated ability to organize and prioritize a complex and dynamic workload
Ability to multitask and meet deadlines, despite interruptions
Ability to prioritize assignments and achieve high productivity/quality with short time frames, under rigid deadlines, and /or in environments with frequent workload changes and competing demands
Skill in working independently, taking initiative and following through on assignments
Ability to work within a deadline-driven structure
Demonstrated experience in maintaining flexibility and adaptability while implementing institutional change
1-3 Years of related clinical research coordination work experience with Bachelor of Arts/Bachelor of Science, or equivalent experience
Experience with cancer-related research.
Knowledge with various types of human subject clinical trials i.e., National Group, industrial, and Investigator-authored.

Preferred:

Experience with clinical trial management systems, preferably OnCore

Special Conditions:

May require travel to satellite sites.
May require study management coordination outside of normal business hours.

Total Compensation

In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our compensation practices and benefits.

The expected pay range for this recruitment is $27.40- $34.43 (Hourly).

Conditions of Employment:

The University of California, Irvine (UCI) seeks to provide a safe and healthy environment for the entire UCI community. As part of this commitment, all applicants who accept an offer of employment must comply with the following conditions of employment:

Background Check and Live Scan
Legal Right to work in the United States
Vaccination Policies
Smoking and Tobacco Policy
Drug Free Environment

The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements.

California Child Abuse and Neglect Reporting Act
E-Verify
Pre-Placement Health Evaluation

Details of each policy may be reviewed by visiting the following page - https://hr.uci.edu/new-hire/conditions-of-employment.php

Closing Statement:

The University of California, Irvine is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.

For the University of California’s Affirmative Action Policy please visit: https://policy.ucop.edu/doc/4010393/PPSM-20.

For the University of California’s Anti-Discrimination Policy, please visit: https://policy.ucop.edu/doc/1001004/Anti-Discrimination.

We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.
UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824-0500 or [email protected].

Apply Now

Refine Your Search

investigator assistant jobs in orange county ca

ASST. RESEARCH DATA COORDINATOR - HYBRID

Investigative Assistant I/II

Asset Protection Investigator

Asst. Clinical Research Coordinator - Hybrid

Regulatory Affairs Coordinator

Research Assistant II

Dental Assistant II - Correctional Health Services

Physician Assistant

Clinical Research Site Manager

Clinical Research Assistant

Regulatory Affairs & Quality Assurance Manager

Beall Applied Innovation Assistant Director, Licensing

Sub-Investigator (NP or PA) - Westside Los Angeles

Health Services Manager, Senior

Clinical Research Manager

Psychiatrist - CHS

Post-Doctoral Research Scientist – RNA Analysis

Post-Doctoral Research Scientist - RNA Analysis

Director of Psychiatric Mental Health Nurse Practitioner Program

Clinical Research Coordinator Manager - Oncology

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