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claims investigator - full time

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field aoe coe investigator

CalStar Unlimited

CalStar Unlimited (CA PI# 187978), a growing private investigative firm focused on insurance investigations, is looking to hire an experienced AOE/COE Investigator based in the greater Los Angeles, California area.An AOE/COE Investigator will conduct compensability investigations for workers&rsquo; compensation claims. Typical activities will include conducting thorough recorded interviews with various subjects, canvassing locations to develop witnesses and/or information, obtaining photographic and video evidence, and securing necessary documentation from public and private sources, with all results being documented in a comprehensive written report. CalStar Unlimited has carved out a niche in the industry as being a high-quality, results-oriented investigative company, and we are looking for someone who can perform the above services at an above-average level.The position will be based in or near Los Angeles, and the service area will include various locations in Los Angeles County, as well as the surrounding counties. The wage for this position is based on experience and qualifications.The ideal candidate will possess the following characteristics:- One or more years of experience conducting AOE/COE investigations- An independent worker with integrity, a commitment to producing good work, and the ability to make sound decisions in the field- Effective oral communication skills and a personable demeanor, with the ability to solicit information from individuals of varying backgrounds- Excellent writing skills, with the ability to create reports that adhere to an established style and format.- Fluency in Spanish is desired, but not required.To be considered, please submit a resume explaining why you are an ideal candidate for the position.Job Types: Full-time, Part-timePay: From $29.00 per hourBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Vision insurance</li></ul>Work Location: Remote

Field (AOE/COE) Investigator

Chubb Insurance

<div>Chubb is currently seeking a Workers&rsquo; Compensation Medical Only Claim Examiner for our West Coast/Pacific region. The successful applicant will be handling claims from California. The position will report and reside in our Los Angeles, CA office.
Duties &amp; Responsibilities:
<ul><li>Handles all aspects of workers&rsquo; compensation medical only claims from set-up to case closure ensuring strong customer relations are maintained throughout the process.
</li><li>Review and assess new medical-only claims to determine eligibility and coverage under workers' compensation policies and complete coverage match where necessary.
</li><li>Conducts initial and ongoing investigations, obtaining facts and takes statements as necessary, with insured, claimant and medical providers.
</li><li>Evaluates the facts gathered through the investigation to determine compensability of the claim or if additional investigation for AOE/COE investigation.
</li><li>Coordinate and authorize appropriate medical treatment for injured workers, ensuring timely and effective care.
</li><li>Sets timely reserves within authority limits for medical and expenses and recommends reserve changes to Team Leader throughout the life of the claim.
</li><li>Reviews the claim status at regular intervals and makes recommendations to Team Leader to discuss problems and remedial actions to resolve them.
</li><li>Prepares and submits to Team Leader unusual or possible undesirable exposures when encountered.
</li><li>Controls and directs vendors, telephonic cases managers, and use all medical cost containment programs.
</li><li>Complies with customer service requests including Special Claims Handling procedures, file status notes and claim reviews.
</li><li>Files workers&rsquo; compensation forms and electronic data with states to ensure compliance with statutory regulations.
</li><li>Works with in-house Technical Assistants, Special Investigators, Nurse to exceed customer's expectations for exceptional claims handling service.
</li><li>Always maintains 100%+ closing rate.
</li><li>Timely recommend transfer of claims to lost time status.
</li><li>Maintain detailed and accurate records of all claim activities, including medical reports, correspondence, and payment information.
</li><li>Serve as the primary point of contact for claimants, medical providers, and employers, providing updates and information as needed.
</li><li>Address and resolve any issues or disputes related to medical treatment or claim processing.
</li></ul>Technical Skills &amp; Competencies:
<ul><li>Preference for prior experience as MO Claim Examiner in workers&rsquo; compensation as a lost time examiner, or similar examiner experience in short-term / long-term disability, auto personal injury protection / medical injury, or general liability claims.
</li><li>Requires basic knowledge of workers&rsquo; compensation statutes, regulations, and compliance. Understanding of workers' compensation laws and medical terminology.
</li><li>Exceptional customer service and focus.
</li><li>Ability to openly collaborate with leadership and peers to accomplish goals.
</li><li>Demonstrates a commitment to a career in claims.
</li><li>Exceptional time management and multi-tasking capabilities with consistent follow through to meet deadlines.
</li><li>Use analytical skills to find mutually beneficial solutions to claim and customer issues.
</li><li>Conscientious about the quality and professionalism of work product and relationships with co-workers and clients.
</li><li>Willing to take ownership and tackle obstacles to meet Chubb's quality
</li><li>standards for service, investigation, reserving, inventory management, teamwork, and diversity appreciation.
</li><li>Superior verbal and written communication skills.
</li><li>High school diploma or equivalent; some positions may require an associate's or bachelor's degree in a related field.
</li></ul>Experience, Education &amp; Requirements:
<ul><li>Experience working in a customer focused, fast-paced, fluid environment
</li><li>Experience utilizing strong communication and telephonic skills
</li><li>Prior experience requiring a high level of organization, follow-up, and accountability
</li><li>Prior workers&rsquo; compensation claim handling experience or other similar type of claim handling experience is preferred (healthcare, short-term / long-term disability, auto personal injury protection / medical injury, or general liability).
</li><li>Proficiency with Microsoft Office Products
</li><li>If you do not already have one, you will be required to obtain an applicable resident or designated home state adjusters license and possibly additional state licensure.
</li></ul>The pay range for the role is $57,200 to $83,300. The specific offer will depend on an applicant&rsquo;s skills and other factors. This role may also be eligible to participate in a discretionary annual incentive program. Chubb offers a comprehensive benefits package, more details on which can be found on our careers website . The disclosed pay range estimate may be adjusted for the applicable geographic differential for the location in which the position is filled.</div>
 <div><div>Chubb is a world leader in insurance. With operations in 54 countries, Chubb provides commercial and personal property and casualty insurance, personal accident and supplemental health insurance, reinsurance, and life insurance to a diverse group of clients. The company is distinguished by its extensive product and service offerings, broad distribution capabilities, exceptional financial strength, underwriting excellence, superior claims handling expertise and local operations globally. 
</div><div></div> 
<div>At Chubb, we are committed to equal employment opportunity and compliance with all laws and regulations pertaining to it. Our policy is to provide employment, training, compensation, promotion, and other conditions or opportunities of employment, without regard to race, color, religious creed, sex, gender, gender identity, gender expression, sexual orientation, marital status, national origin, ancestry, mental and physical disability, medical condition, genetic information, military and veteran status, age, and pregnancy or any other characteristic protected by law. Performance and qualifications are the only basis upon which we hire, assign, promote, compensate, develop and retain employees. Chubb prohibits all unlawful discrimination, harassment and retaliation against any individual who reports discrimination or harassment.</div></div>

Claim Representative

CoventBridge Group

<div>Overview:

Claims Investigator &ndash; Full Time
Los Angeles, CA 
Uncover the Truth. Protect the Integrity. Advance Your Career. 
At CoventBridge Group, every claim tells a story &mdash; and as a Claims Investigator, you&rsquo;ll be the one uncovering it. Using your investigative instincts, field experience, and attention to detail, you&rsquo;ll help clients get the answers they need and ensure claims are resolved with accuracy and fairness. 
Join a global leader in full-service investigations, where integrity meets action, and every day brings a new case &mdash; and a new challenge. 
At this time, CoventBridge is not considering candidates who require visa sponsorship, currently or in the future, including but not limited to H-1B, H-2B, E-3, TN, O-1, F-1 (OPT/CPT, or J-1 Visa Statuses.)
Responsibilities/ Requirements:

What You&rsquo;ll Do:
As a Claims Investigator, you&rsquo;ll combine analytical skill with real-world investigation techniques to uncover facts, document findings, and deliver objective results. You will:<ul><li>Conduct complex field investigations involving multiple claim types.</li><li>Submit daily updates summarizing your progress and observations.</li><li>Manage your time effectively to maintain client billable hour expectations.</li><li>Write detailed, professional statements and investigative summaries.</li><li>Deliver clear, client-ready reports that meet CoventBridge&rsquo;s quality standards.</li><li>Perform scene investigations, background checks, and courthouse research.</li><li>Operate safely and remain alert while driving during field assignments.</li></ul>
Your curiosity and persistence will turn each case into a story built on truth and evidence. 
What You&rsquo;ll Bring:
We&rsquo;re looking for investigators who are driven, professional, and dedicated to uncovering facts with accuracy and integrity.<ul><li>Hold a valid (state) Investigator license (or eligibility for licensure in surrounding states).</li><li>Demonstrate at least 1 year of field investigations experience, including face-to-face statements and report writing.</li><li>Travel across multiple states as needed to complete case assignments.</li><li>Investigate claims related to product, auto, general liability, Workers&rsquo; Compensation, disability, life insurance, and contestable death cases.</li><li>Adapt to variable schedules &mdash; including nights and weekends when required.</li><li>Maintain a reliable, fuel-efficient vehicle and required insurance coverage.</li><li>Equip yourself with a digital recorder, laptop (Windows OS), and necessary investigative tools.</li></ul> 
What You&rsquo;ll Need:
To qualify for this position, applicants must possess the following:<ul><li>A minimum of 3-5 years of Claims, SIU, or adjusting experience.
</li><li>An Associate&rsquo;s or Bachelor&rsquo;s degree in Criminal Justice or a related field.</li><li>Strong report writing skills.</li><li>Understand investigative processes, insurance law, and claim procedures.</li><li>Excel in report writing and typing (50+ WPM) with accuracy and attention to detail.</li><li>Thrive under pressure and maintain professionalism in sensitive situations.</li><li>Demonstrate self-motivation, accountability, and sound judgment.</li></ul>
Benefits:

Benefits
We believe great work deserves great rewards. Here&rsquo;s what you can expect when you join our team:<ul><li>Home-based work and flexible scheduling</li><li>Competitive pay with monthly vehicle allowance</li><li>Paid time off</li><li>Company fuel card and company-issued cell phone</li><li>Medical, Dental, Vision plans</li><li>Employer-paid Life, LTD, STD insurance</li><li>401(k) with company match</li><li>Travel and report writing compensation</li><li>Licensing fees paid by company</li><li>Paid ongoing career advancement training</li><li>Expense reimbursement with minimal out-of-pocket expenses</li></ul><div> 
The salary range for this role is $27-$30 per hour. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. An employee&rsquo;s pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs.</div><div> 
</div><div>Pursuant to the respective Fair Chance Ordinances of both Los Angeles and San Francisco, we will consider for employment qualified applicants with arrest and conviction records.</div> 
About Us:
CoventBridge Group is a global leader in full-service investigations providing: Surveillance, SIU and Compliance, Claims Investigation, Counter-Fraud Programs, Desktop Investigations, Social Media, Record Retrieval, Canvasses and Vendor Management programs. The company provides top tier data privacy and security practices, deploys robust case management technology customized to clients&rsquo; needs and delivers worldwide coverage via its 700+ employees and affiliates worldwide. 
CoventBridge is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, caste, disability, veteran status, and other legally protected characteristics and maintains a drug-free workplace. 
CoventBridge is committed to the full inclusion of all qualified individuals. As part of this commitment, CoventBridge will ensure that persons with disabilities are provided reasonable accommodations. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: Human Resources; 888-932-7364; humanresources@coventbridge.com. 
CoventBridge Group Inc. California License # PI27136</div>

Claims Investigator - Full Time

Advantage Investigations

<div><div>For the past 28 years, Advantage Investigations has been the Nation&rsquo;s only insurance defense investigation firm that invests in the operational capabilities necessary to produce consistent, high-quality results&mdash;ultimately helping our clients &quot;See What&rsquo;s True.&quot;</div><div></div><div> 
With over 200+ licensed private investigators Nationwide, Advantage uses strategic planning and technology to give our clients greater clarity on a claimant's daily activities. Providing Covert Surveillance, Claims Investigations, Net-Sweep Investigations, Remote Controlled Surveillance, and more, we&rsquo;re able to save our clients time and money on insurance fraud cases.</div><div></div> 
Advantage Investigations is seeking a Full-Time (will also consider PT) SIU/Claims Investigator in Los Angeles, CA/Surrounding Areas. The qualified candidate will be responsible for conducting investigations of auto, property, homeowner liability and worker&rsquo;s compensation insurance claims in support of client objectives and Company quality standards. As an SIU/Claims Investigator, you will be provided with a comprehensive training program, door to door pay, and mileage reimbursement at the IRS rate. This position requires daily travel within the investigator&rsquo;s area/territory.<div> 
Duties &amp; Responsibilities:</div><div><ul><li>
Conduct investigations of auto, property, liability, and worker&rsquo;s compensation claims</li><li>
Independently reviews the assignment, supporting documentation and all other case information prior to commencing the on-site assignment.</li></ul></div><ul><li>
Consults with the Manager on appropriate strategies for individual cases, before and throughout the investigative process.</li><li>
Locate subjects of the assigned investigation and conduct applicable case investigation, to include recorded statements and scene investigations etc.</li><li>
Creates and maintains written daily updates, supporting photos, audiotapes, diagrams, and final investigative reports for in a timely and professional manner</li><li>
Time management and communication skills</li><li>
Ability to handle confidential information and material</li></ul> 
Qualifications &amp; Requirements:<ul><li>
3 years claims investigative experience preferred</li><li>
3 years investigative experience required</li></ul><div><ul><li>
Bi-Lingual a plus</li></ul></div><ul><li>
Private Investigator License required in most states</li></ul><ul><li>
Full comprehension of case management systems</li><li>
Able to proactively conduct follow-ups as needed</li><li>
Good Oral and Written Communication Skills</li><li>
Proficient in computer technology &ndash; including Microsoft office type products, email, and the ability to produce quality, well-written reports</li><li>
Self-Starter/Disciplined work ethic with ability to ask relevant questions when needed, and work indecently</li><li>
Meet state mandated requirements to obtain and maintain a Private Investigator license multiple states</li><li>
Daily access to a reliable vehicle</li><li>
Valid Driver&rsquo;s License</li><li>
Ability to provide MVR (driving record)</li><li>
Pass Drug Screen</li></ul> 
Compensation: Investigators are paid door to door an hourly rate commensurate with experience within $25.00 to $30.00 an hour. Employees are paid on a bi-weekly basis. 
Company Benefits:<ul><li>
Door to Door hourly pay</li><li>
Mileage Reimbursement at IRS rate</li><li>
401k with match</li><li>
Flexible Schedule</li></ul> 
Advantage Investigations 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 or protected veteran status.</div>

SIU Investigator

UCLA Health

<div><div>Description
The Department of Medicine, Division of Cardiology, is seeking a Research Nurse Coordinator to support cardiovascular clinical trials and innovative research initiatives. Under the direction of the Principal Investigator, this role performs independent nursing and advanced administrative duties to ensure the effective implementation and management of clinical research protocols. Responsibilities include seeing research participants, reviewing safety labs and adverse events, implementing investigational drug dose adjustments per protocol, and performing specialized clinical procedures such as electrocardiograms, spirometry, and cardiopulmonary exercise testing while monitoring vital signs.
This position supports a diverse portfolio of studies, including multicenter NIH and industry-sponsored trials, investigator-initiated research, and programmatic activities such as clinical databases and biorepositories. The Research Nurse Coordinator works closely with investigators, clinicians, research staff, and external partners to ensure regulatory compliance, patient safety, and efficient study operations while contributing clinical expertise to the advancement of cardiovascular research.
*This is a limited role which may convert to career.*
Hourly range: $70.59-$106.80</div><div>
Qualifications
<div>Required:</div><div></div><ul><li>
BSN or MSN &ndash; required</li><li>
Active California Registered Nursing License</li><li>
5 years of Cardiovascular Research experience</li><li>
ACLS, BCLS and PALS from the American Red Cross or American Heart Association &ndash; required</li><li>
Ability to complete a Nursing physical assessment</li><li>
Ability to conduct cardiopulmonary exercise testing</li><li>
Ability to complete research case report forms and other research-related documentation according to good clinical practice (GCP) standards and regulatory requirements</li><li>
Ability to follow research standard operating procedures and study protocols</li><li>
Working knowledge of HIPPA guidelines and Human Subjects Protection rights.</li></ul></div></div><div></div>

Research Nurse Coordinator (20% Limited)

Thermo Fisher Scientific

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Fluctuating Temps hot/cold
Job Description
Join Us as a Senior Clinical Research Associate (Level I) &ndash; Make an Impact at the Forefront of Innovation 
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
 
 
As part of our global team, you&rsquo;ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix. 
 
What You&rsquo;ll Do: 
<ul><li>Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable</li><li>Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.</li><li>Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.</li><li>Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.</li><li>Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).</li><li>Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.</li><li>Responds to company, client and applicable regulatory requirements/audits/inspections.</li><li>Maintains &amp; completes administrative tasks such as expense reports and timesheets in a timely manner.</li><li>Contributes to other project work and initiatives for process improvement, as required.</li></ul> 
Education and Experience Requirements:
 
<ul><li>Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
</li><li>Valid driver's license where applicable</li><li>In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
</li></ul> 
Knowledge, Skills and Abilities:
 
<ul><li>Effective clinical monitoring skills</li><li>Demonstrated understanding of medical/therapeutic area knowledge and medical terminology</li><li>Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents</li><li>Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving</li><li>Ability to manages Risk Based Monitoring concepts and processes</li><li>Effective oral and written communication skills, with the ability to communicate effectively with medical personnel</li><li>Ability to maintain customer focus through the utilization of good listening skills, attention to detailand the ability to perceive customers&rsquo; underlying issues</li><li>Effective interpersonal skills</li><li>Strong attention to detail</li><li>Effective organizational and time management skills</li><li>Ability to remain flexible and adaptable in a wide range of scenarios</li><li>Ability to work in a team or independently as required</li><li>Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software</li><li>Good English language and grammar skills</li><li>Good presentation skills</li></ul> 
Working Conditions and Environment:
 
<ul><li>Working Conditions and Environment:</li><li>Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.</li><li>Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.</li><li>May also include extended overnight stays.</li><li>Exposure to biological fluids with potential exposure to infectious organisms.</li><li>Personal protective equipment required such as protective eyewear, garments and gloves.</li><li>Exposure to fluctuating and/or extreme temperatures on rare occasions.</li><li>Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.</li></ul></div>

Senior CRA

<div><div>Description
Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health&rsquo;s world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.

The incumbent will support a wide range of clinical research activities under the guidance of the Principal Investigator. Responsibilities include managing human subject regulatory requirements&mdash;such as ARC and IRB submissions, tracking adverse events, ensuring FDA compliance, and coordinating DSMB activities. The role also oversees participant recruitment, screening, enrollment, and retention. Additional duties include organizing and analyzing study data, generating summary figures and tables, contributing to presentations and manuscripts, and reviewing and entering chart data into study databases. Prior research experience is preferred, and experience coordinating multi site clinical studies is highly beneficial. All work will be performed under the supervision of the Principal Investigator or senior scientific staff.

Salary: $31.21 - $50.21 hourly</div><div>
Qualifications
Required:<ul><li>
Excellent skills in computer and software operation 
</li><li>
Knowledge and experience using word processing, spreadsheet (Microsoft Word/Excel) 
</li><li>
Proven track record of working with high level of accuracy. 
</li><li>
Demonstrated ability to write clear, concise, and grammatically correct letters, memos, and emails. 
</li><li>
Excellent ability to perform a variety of duties with frequent interruptions and to work effectively under conditions of fluctuating workload. 
</li></ul><div>
Preferred: 
</div><div><ul><li>
Bachelor&rsquo;s Degree and/or equivalent combination of education and experience. 
</li><li>
Previous experience in data management of clinical research protocols, including the completion of case report forms and other study documents. 
</li><li>
Knowledge of health services or clinical research methodology and principles. 
</li><li>
Prior IRB experience and coordination of clinical studies desired. 
</li><li>
Experience working with a diverse research population. 
</li><li>
Knowledge of simple statistical analysis. 
</li><li>
Excellent scientific writing skills in order to write or edit correspondence, progress reports, and research papers 
</li><li>
Knowledge and experience using statistical analysis software 
</li><li>
Knowledge of basic statistical tests and procedures related to data management and selection of descriptive tests for summarizing data. 
</li><li>
Knowledge of the rules and regulations for Human Subject Protection and informed consent</li></ul></div></div></div><div></div>

Staff Research Associate II - VA

Explore 289+ Field aoe coe investigator in Los Angeles this March. Find roles across top companies and apply now to boost your career.