Research Administrator
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Research Administrator at University of California, Irvine summary:
The Research Administrator at UC Irvine supports the development and management of research grants and contracts by coordinating proposals, overseeing compliance, and handling financial administration. This role requires expertise in federal and non-federal research funding mechanisms, regulatory compliance, financial analysis, and reporting. The incumbent acts as a technical leader managing complex research portfolios and ensuring adherence to institutional policies and sponsor regulations.
Who We AreFounded 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 in 1968, the UCI School of Medicine Department of Biological Chemistry boasts a rich legacy of pioneering research into the fundamental building blocks of life. Our dedication to basic science research fuels advancements in medicine and cultivates a collaborative environment for scientists to flourish.
Your Role on the Team
The position involves providing analytical, financial and training activities in support of contract and grant proposal development, grant-writing, funding, administration, and budget development. Activities may include pre-award proposal initiatives, management of funds post-award, and closeout activities for federal, state, local and private sponsors. Involves activities associated with analyzing research funding trends and sources, forecasting, planning, and managing of research portfolios by performing some or all of the following: coordinating and identifying and developing and / or presenting proposals, contracts and other agreements; reviewing proposals to ensure institutional compliance and program success; administering and monitoring contract and grant awards, including compliance with regulations, terms and conditions; financial management and reporting; and sub award / subcontract issuance and administration.
Incumbent will be a technical leader with a high degree of knowledge in the overall field and recognized expertise in specific areas; problem-solving frequently requires analysis of unique issues / problems without precedent and / or structure. May manage programs that include formulating strategies and administering policies, processes, and resources; functions with a high degree of autonomy.
Uses advanced contracts and grants concepts to manage high volume and high complexity transactions. May review and guide others in the review of financial and administrative management requirements of research contract and grant proposals, awards, and / or transactions to ensure compliance with institutional and sponsor policies. Works independently to assess complex grant, contract and subcontract transactions where analysis requires an in-depth evaluation of variable factors. May be eligible for delegated signature authority. May review and sign transactions for less experienced staff. May serve as a technical specialist in a particular area, such as federal contracts, state contracts, subcontracts or information systems. Central Role (CR): Typically works on highly complex proposals and awards such as grants / contracts which require task budgets, option years, multiple investigators and multiple sub awards.
What It Takes to be Successful
Required:
- Extensive knowledge of program administration guidelines of Federal and non-Federal sponsors supporting research and educational activities, preferably in a university environment.
- Thorough knowledge of applicable compliance requirements related to use of human or animal subjects in research, financial conflict of interest, biosafety, etc.
- Advanced knowledge of applicable compliance requirements related to use of human or animal subjects in research, financial conflict of interest, biosafety, etc.
- Ability to manage high volume and complex transactions.
- Ability to perform highly complex financial analysis and customized reporting.
- Demonstrated advanced competence in the use of spreadsheet and database software in financial analysis, fiscal management and financial reports
- Ability to maintain independent judgment; strong organization and communication skills; and a customer service focus across broad and diverse subject areas.
- Maintains knowledge of and ability to interpret and apply sponsor, institutional and departmental policies. Knowledge of current compliance regulations in all areas of research administration.
- Demonstrated advanced knowledge of generally accepted accounting, fiscal and reporting principles.
- Experience with all types of award mechanisms, including grants, contracts, subcontracts, and cooperative agreements
- Full knowledge of Federal Acquisition Regulation, Code of Federal Regulations, sponsor-specific policies, intellectual property policy, conflict of interest requirements, publication rights, application of indirect cost rates and other complex concepts in research administration.
- Ability to interpret policy for others.
- Advanced knowledge of effective grant funding processes, procedures and techniques
- Advanced ability to create and train grant writing and other communications skills in a variety of styles to ensure securing grant funding required.
- Bachelor's degree in related area and / or equivalent experience / training
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.
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
- Employment Misconduct*
- Legal Right to work in the United States
- Vaccination Policies
- Smoking and Tobacco Policy
- Drug Free Environment
*Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
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 - Statement:
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC Anti-Discrimination Policy.
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 or
Consideration for Work Authorization Sponsorship
Must be able to provide proof of work authorization
Keywords:
research administration, grant management, contract compliance, financial analysis, budget development, proposal coordination, federal funding, regulatory compliance, sponsor reporting, research portfolio management
Research Director

Posted 2 days ago
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Job Description
Job ID
Posted
23-Sep-2025
Service line
Advisory Segment
Role type
Full-time
Areas of Interest
Research
Location(s)
El Segundo - California - United States of America, Glendale - California - United States of America, Irvine - California - United States of America, Los Angeles - California - United States of America, Ontario - California - United States of America
About The Role:
As a CBRE Research Director, you will oversee the work of the Los Angeles region (greater LA, Orange County and Inland Empire) research team, to collect market intelligence and deliver actionable and valuable insights to local business leadership, sales professionals and clients. We are looking for an outgoing, articulate and dynamic research leader who can be a partner in improving the platform, interacting with clients, and helping local sales professionals win business and drive revenue growth.
What You'll Do:
Partnership, engagement and expertise:
- Regularly engage with market leaders and key brokers to gather feedback on research support at the point of sale, ensure strategic alignment of research priorities and initiatives, and identify areas of improvement.
- Participate in kickoff meetings for key pitches and pursuits, mobilize team resources to meet the specific needs of pitches and pursuits, and present research findings to clients.
- Confidently engage with clients and collaborate with the sales team to craft and deliver compelling market narratives during pitches and client presentations.
- Cultivate strong working relationships with Los Angeles-area business publications and trade organizations by actively seeking speaking opportunities to amplify the CBRE brand and establishing CBRE as leading resource for these organizations.
Manager of local data operations and research report outputs:
- Ensure data integrity and lead local data collection efforts by maintaining and updating a proprietary database with real estate market data, including, but not limited to, availability, vacancy and lease rates, lease and salecomparables, development activity, and tenant occupancy.
- Coordinate the delivery and updates of standard Field Research outputs such as quarterly Figures reports, building stacks and skylines, and market overviews.
- Collaborate with local leadership and national thought leaders on a thoughtful agenda of local content and reports focused on compelling real estate and economic trends.
- Provide key insights and implications for commercial real estate.
Leader and people manager for the Los Angeles area research team:
- Responsible for hiring, budgeting, task delegation, and project deadlines.
- Provide formal supervision to individual employees within the research team.
- Plan and monitor appropriate staffing levels and utilization of labor, including overtime.
- Prepare and deliver performance appraisal for staff.
- Mentor team members to foster their professional development and enhance their proficiencies.
- Perform other duties as assigned.
What You'll Need:
To perform this job successfully, an individual will need to perform each crucial duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
_Applicants must be currently authorized to work in the United States without the need for visa sponsorship now or in the future._
- Bachelor's degree required, Master's degree preferred.
- 10+ years of experience in commercial real estate, with a minimum of 3 years of experience leading and managing a team.
- Excellent written and verbal communication skills. Must be able to prepare and deliver effective and persuasive presentations on complex topics to employees, clients, top management and/or public groups.
- Outgoing and capable of establishing relationships that enable collaboration as well as the gathering of market intelligence. Ability to build trust and rapport internally with sales team and other internal and external business partners across the market.
- Ability to respond to the most critical issues and exercise discretion and sound judgment.
- Ability to motivate and negotiate with key employees, top management, and client groups to take desired action.
- Expertise on the California real estate market. In-depth knowledge of commercial real estate terms and principles. Ability to calculate complex figures. Conducts business analysis including the preparation of reports.
- Ability to solve advanced problems and take care of a variety of options in complex situations.
- Requires expert level analytical and quantitative skills with proven experience in developing strategic solutions for a growing matrix-based multi-industry sales environment. Draws upon the analysis of others and develop recommendations that have a direct impact on the company.
- Advanced experience with Microsoft Office Suite. Comfortable using dashboard software such as Tableau or Power BI.
- Knowledge of Company research systems as well as internal and external information sources.
Why CBRE?
When you join CBRE, you become part of the global leader in commercial real estate services and investment that helps businesses and people thrive. We are dynamic problem solvers and forward-thinking professionals who create significant impact. Our collaborative culture is built on our shared values - respect, integrity, service and excellence - and we value the diverse perspectives, backgrounds and skillsets of our people. At CBRE, you have the opportunity to chart your own course and realize your potential. We welcome all applicants.
Our Values in Hiring
At CBRE, we are committed to fostering a culture where everyone feels they belong. We value diverse perspectives and experiences, and we welcome all applications.
About CBRE Group, Inc.
CBRE Group, Inc. (NYSE:CBRE), a Fortune 500 and S&P 500 company headquartered in Dallas, is the world's largest commercial real estate services and investment firm (based on 2024 revenue). The company has more than 140,000 employees (including Turner & Townsend employees) serving clients in more than 100 countries. CBRE serves clients through four business segments: Advisory (leasing, sales, debt origination, mortgage serving, valuations); Building Operations & Experience (facilities management, property management, flex space & experience); Project Management (program management, project management, cost consulting); Real Estate Investments (investment management, development). Please visit our website at carefully considers multiple factors to determine compensation, including a candidate's education, training, and experience. The minimum salary for the Research Director position is $130,000 annually and the maximum salary for the Research Director position is $170,000 annually. The compensation that is offered to a successful candidate will depend on the candidate's skills, qualifications, and experience.
Successful candidates will also be eligible for a discretionary bonus based on CBRE's applicable benefit program. This role will provide the following benefits: 401(K), Dental insurance, Health insurance, Life insurance, and Vision insurance.
**Equal Employment Opportunity:** CBRE has a long-standing commitment to providing equal employment opportunity to all qualified applicants regardless of race, color, religion, national origin, sex, sexual orientation, gender identity, pregnancy, age, citizenship, marital status, disability, veteran status, political belief, or any other basis protected by applicable law.
**Candidate Accommodations:** CBRE values the differences of all current and prospective employees and recognizes how every employee contributes to our company's success. CBRE provides reasonable accommodations in job application procedures for individuals with disabilities. If you require assistance due to a disability in the application or recruitment process, please submit a request via email at or via telephone at (U.S.) and (Canada).
CBRE, Inc. is an Equal Opportunity and Affirmative Action Employer (Women/Minorities/Persons with Disabilities/US Veterans)
Clinical Research Specialist
Posted today
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Job Responsibilities :
- Manage & coordinate in-house clinical ops
- Act as site manager and company interface for active studies
- Responsible for site regulatory document collection, filing of study documents in trial master file (TMF), ICF review/approval, IRB/EC submission (including annual submissions), payments tracking, study supply management (as appropriate), study communication, field training and support
- Responsible for implementation of clinical study documents as needed, including but not limited to: ICFs, amendments to study protocols, SOPs, Work Instructions (WIs) and study-specific forms, to ensure appropriate compliance with site start-up and initiation process and applicable regulations
- Review sample, investigator-prepared and IRB-approved informed consents
- Support the design, format and content of study guides and subject instructions
- Coordinate activities associated with site startup
- Interface with in-house data and EDC/CTMS management to ensure seamless study execution
- Support clinical dossier preparation for CEC meetings
- Support prep of clinical sites for regulatory inspections
- Partner with and work cross-functionally with various team members
Job Requirements :
- 4+ years prior experience in clinical ops role – experience in Med Device or Spine industry strongly preferred
- Ability to travel for monitoring or as requested by the study team
- Strong project management skills with an entrepreneurial attitude
- Proficient with clinical trial management software including EDC, eTMF, CTMS
- Prior experience with IDE clinical trial and international regulatory process required including FDA; ICH and ISO:14155.
- Strong communication & problem-solving skills
- Self-motivated, team player, with excellent time management skills
Research Associate (Large Animals)
Posted today
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Medical Affairs Research Associate
Hybrid - Onsite in Irvine, CA Tuesday/Thursday and every other Friday
Weekends, Domestic travel will be required up to 40%, occasional weekends
Essential Duties & Responsibilities:
- Independently works on in-vivo and bench models for the investigation of cardiac products and how they perform in a simulated clinical use setting.
- Independently identifies data outliers, prepares data for statistical analysis for in-vivo study data
- Assists in in-vivo protocol execution, may develop or be a part of developing new processes/test fixtures or methods for medical device testing
- Interfaces with internal customers within R&D, Medical Safety, and Quality
- May be asked to assist in model development for proper statistical analysis of in-vivo, clinical, and other parametric datasets
- May be asked to assist in the production of mathematical and/or computational modeling of cardiac systems using electromechanical design and controls
- Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance as well as develop a strong working knowledge of design controls and quality assurance standards of procedure.
- Has a working knowledge of good laboratory practices and operating room procedures
- Willingness to develop an understanding of cardiac electrophysiology procedures and the products used
- Excellent oral and written communication skills are required
Qualification Requirements:
- Experience in working with soft tissue (handling, histology and fixation, including staining and dissection). Previous experience with Bioinstrumentation laboratory equipment.
- Experience in working with large animal (porcine/ovine, etc) and bench top models.
- Strong working knowledge with all of the programs listed: MicroSoft office (specifically Excel and PowerPoint), statistical analysis tools (such as SAS or Minitab, R, SPSS), and working knowledge of Mathematical modeling MatLab software or Prism Job Description
Education & Experience:
- A minimum MS in the Sciences or Engineering or equivalent from an accredited Laboratory Science program, College or University.
- At least 5-8 years of Laboratory experience (Industry and/or Hospital); and/or related medical device development experience and/or training is required. Experience in cardiology, cardiac biophysics and anatomy are preferred
Research And Development Specialist
Posted today
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Our client is a quickly growing Food Production Brand who is looking for a Research and Development Specialist. The R&D Specialist will focus on providing expertise in developing new food products from concept to production. This is a newly created role with HEAVY growth potential!
**this role is on site**
Research and Development Specialist (On Site - Norwalk):
- Must have experience in culinary R&D and product innovation
- Must have QSR (Quick Service Restaurant) experience either in fast food, grab and go or grocery/convenience
- Must have strong working knowledge of formulation of fresh food products and shelf-life extension
- Must have an understanding traditional techniques, ingredients, and flavors, combined with the ability to experiment with new elements
- Will spearhead the creation of new product development
- Will research and identify emerging product trends
- Salary likely to be $110k-$135k + bonus, benefits, PTO
There is a ton of growth opportunity in this position, and a great team around them. The company is built around fun, devoted people, who love the brand and work hard to promote and grow it. They have a lot of stability within their group, and are excited to add another great member to the team.
If interested, please attach a WORD DOC version of your resume in your reply. We look forward to
chatting with you soon. Thanks for your time!
Pharmacy Tech - Clinical Research
Posted 3 days ago
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Job Description
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Hourly Range: 21.00 - 23.00/hr ( Depending on education, experience, and skillset)
Schedule: ( 8:00 am to 4:30 pm) Monday - Friday + must be able to work rotating weekends.
Job Summary:
With moderate oversight, the Pharmacy Technician I will assist in providing support of clinical investigational drug trials; provide accurate and efficient dispensing of medication, and perform cross-functional duties as required.
Essential Responsibilities and Duties:
- Monitors pharmacy activities daily to ensure adherence to study protocols and dispensing procedures.
- Prepare and dispense investigational drugs in accordance with the IRB-approved protocols under the supervision of the Pharmacist or site management.
- Assist Pharmacist or site management in preparing blinded study products.
- Ensure the appropriate storage of investigational drugs according to the protocol and FDA guidelines.
- Monitor temperature of pharmacy storage areas and alert Pharmacist or site management of any temperature excursions of study drug.
- Assists in ordering, receiving, unpacking and storing pharmaceuticals and supplies.
- Rotates stock to ensure use before expiration date.
- Monitors expiration date and supply of drug for clinical trials.
- Prepares medication for dispensing to patients enrolled in inpatient study protocols.
- Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
- Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
- Must be able to effectively communicate verbally and in writing.
- Certified Pharmacy Technician required.
- Minimum of 1 year related experience preferred.
- Knowledge of basic pharmacy practices and procedures.
- Knowledge of medications and medical supplies.
- Ability to maintain quality control standards.
- Ability to react calmly and effectively in emergency situations.
- Ability to interpret, adapt, and apply guidelines and procedures.
- Attention to detail.
Working Conditions
- Indoor, Clinic environment.
- Essential physical requirements include sitting, typing, standing, walking.
- Lightly active position, occasional lifting of up to 20 pounds.
- Reporting to work, as scheduled, is essential.
- On-site work arrangement.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Clinical Research Coordinator II

Posted 2 days ago
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Job Description
**Kelly® Science & Clinical** is seeking an experienced Clinical Research Coordinator II for a full-time, direct hire opportunity with our client who has been recognized as one of the largest independent, multi-site clinical research companies in the US.
If you are passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust **The Experts at Hiring Experts.**
+ **Location** : Onsite/Newport Beach, CA (additional site coverage needed for Mission Viejo, CA)
+ **Job Opportunity** : Full-Time/Direct Hire
+ **Salary** : $ /Hour (which includes occasional overtime, PTO, and competitive benefit options)
**Position Overview**
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
**Responsibilities**
+ Assisting trial Investigator in screening and reviewing potential study participants eligibility.
+ Maintaining case report forms, charts and documentation.
+ Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants.
+ Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
+ Collecting and entering data as necessary.
+ Assist management with potential new hire selection and shadowing process.
+ Assist with study start-up, maintenance, and close-out of studies as needed for those on the team.
+ Ability to be flexible with study assignments.
**Qualifications**
+ Clinical Research Coordinator with at least two years of relevant experience.
+ Phlebotomy experience is highly preferred.
+ Previous experience as a medical assistant, LPN, or RN.
+ Excellent verbal and written communication skills.
+ Ability to learn quickly, read and understand complex protocols, follow detailed directions, and multi-tasking.
+ Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines.
+ Extensive clinical trial knowledge through education and/or experience.
+ Successful completion of GCP Certification and Advanced CRC preferred.
+ Detail-oriented.
+ Familiarity with the Code of Federal Regulations as they pertain to human subject protection.
+ Strong interpersonal skills.
**Benefits**
A career opportunity with our client offers competitive wages, and benefits such as:
+ 401(k), 401(k) Matching
+ Dental Insurance
+ Disability Insurance
+ Employee Assistance Program (EAP)
+ Flexible Spending Account (FSA)
+ Health Insurance
+ Life Insurance
+ Paid Time Off (PTO)
+ Vision Insurance
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. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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 Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's 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.
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