Centene Corporation is a leading healthcare enterprise committed to helping people live healthier lives. Centene offers affordable and high-quality products to more than 1 in 15 individuals across the nation, including Medicaid and Medicare members (including Medicare Prescription Drug Plans) as well as individuals and families served by the Health Insurance Marketplace.

Centene believes healthcare is best delivered locally. Our local health plans provide fully integrated, high-quality, and cost-effective services to government-sponsored and commercial healthcare programs, focusing on under-insured and uninsured individuals. 

Centene’s hiring practices reflect the composition of the members and communities we serve, allowing us to deliver quality, culturally sensitive healthcare to millions of members. Centene employees help change the world of healthcare and transform our communities. To learn more about career opportunities with Centene, visit: https://jobs.centene.com/

Industry: Hospitals and Health Care
Company Size: 10,001+ employees

Centene Corporation

Savvy Admin PROD

You could be the one who changes everything for our 28 million members. Centene is transforming the health of our communities, one person at a time. As a diversified, national organization, you’ll have access to competitive benefits including a fresh perspective on workplace flexibility.

- Please note Candidates must reside within the state of California*

**Position Purpose **Investigate allegations of potential healthcare fraud and abuse activity. Assist in planning, organizing, and executing claims investigations or audits that identify, evaluate and measure potential healthcare fraud and abuse.

- Conduct investigations of potential waste, abuse, and fraud

- Document activity on each case and refer issues to the appropriate party

- Perform data mining and analysis to detect aberrancies and outliers in claims

- Develop new queries and reports to detect potential waste, abuse, and fraud

- Provide case updates on progress of investigations and coordinate with Health Plans on recommendations and further actions and/or resolutions

- Assist with complex allegations of healthcare fraud

- Prepare summary and/or detailed reports on investigative findings for referral to Federal and State agencies

- Complete various special projects and audits

- Performs other duties as assigned

- Complies with all policies and standards

**Education/Experience **Bachelor's Degree in Business, Criminal Justice, Healthcare, related field or equivalent experience required. 1+ years of medical claim investigation, medical claim audit, medical claim analysis, or fraud investigation experience required.

Pay Range $56,200.00 - $101,000.00 per year

Centene offers a comprehensive benefits package including competitive pay, health insurance, 401K and stock purchase plans, tuition reimbursement, paid time off plus holidays, and a flexible approach to work with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an individual's skills, experience, education, and other job-related factors permitted by law, including full-time or part-time status. Total compensation may also include additional forms of incentives. Benefits may be subject to program eligibility.

Centene is an equal opportunity employer that is committed to diversity, and values the ways in which we are different. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristic protected by applicable law.

Qualified applicants with arrest or conviction records will be considered in accordance with the LA County Ordinance and the California Fair Chance Act

SIU Investigator

ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies. 

With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!

Industry: Business Consulting and Services
Company Size: 5,001-10,000 employees

ProPharma

**Responsibilities **

- Work on investigation burndown plan

- Track current list, schedule and hold daily check-in meetings with the investigators, escalate to upper management and ensure execution (no need to have investigation process background)

- Onsite - Irvine, CA. 3+ months contract.

**Requirement **

- 5-7 years relevant experience

Project Manager

Arc Institute is a new scientific institution that conducts curiosity-driven basic science and technology development.

Headquartered in Palo Alto, California, Arc is a non-profit organization founded on the belief that many important research programs will be enabled by new academic models. Arc operates in partnership with Stanford University, UCSF, and UC Berkeley.

As individuals, Arc researchers collaborate across diverse disciplines to study complex diseases, including cancer, neurodegeneration, and immune dysfunction. As an organization, Arc strives to enable long-term research agendas by betting on people rather than projects, and making it easier to invent and deploy new technologies at scale.

Together, our mission is to accelerate scientific progress, understand the root causes of disease, and narrow the gap between discoveries and impact on patients.

Industry: Biotechnology
Company Size: 51-200 employees

Arc Institute

**About Arc Institute **

Arc Institute is an independent nonprofit research organization at the interface of artificial intelligence and biology, working to accelerate scientific progress and understand the root causes of complex diseases. Founded in 2021 and based in Palo Alto, Arc partners with Stanford University, UC Berkeley, and UC San Francisco.

Unlike academia, our scientists have long-term funding and industry-like resources. Unlike industry, they're free to pursue high-risk, long-term research without commercial pressures. Arc's Technology Centers and Core Investigator labs work side by side, integrating experimental and computational biology under one roof to tackle problems neither could solve alone.

Our two Institute Initiatives reflect this model in action:

- **Virtual Cell Initiative ****: ** Building a full-stack virtual cell model to identify disease mechanisms and nominate drug targets,  accelerating the path from biological insight to clinical trials.

- **Alzheimer's Disease Initiative ****: ** Mapping the genes, pathways, and environmental factors behind Alzheimer's disease to develop drug candidates that address root causes.

More than 300 Arconauts work together at our Palo Alto headquarters, backed by substantial long-term philanthropic funding.

**About the position **

We are seeking a Research Associate I to join the Konermann Laboratory at the Arc Institute. In this position, you will provide essential laboratory support while gaining comprehensive training in lab operations, management, and scientific best practices. You will work closely with our lab manager to support daily operations, maintain high standards of safety and organization, and assist with ongoing research activities. This position is ideal for someone seeking hands-on experience in laboratory operations while contributing to cutting-edge scientific research.

**About you **

- You are naturally proactive with a strong work ethic. You don't wait to be told what needs to be done—you anticipate needs, take initiative, and take pride in maintaining organized, efficient lab spaces. You understand that excellent research depends on meticulous attention to detail and consistent execution.

- You have a natural affinity for process improvement and optimization. You're constantly thinking about how things can be done better, faster, or more efficiently. You enjoy analyzing workflows, identifying bottlenecks, and implementing solutions that benefit the entire team.

- You are collaborative and reliable. You thrive in team environments, take initiative to support others, and can be counted on to follow through on commitments while maintaining excellent communication about priorities and challenges.

- You are motivated by growth and continuous learning. You see this role as an opportunity to develop both technical and operational skills, and you're committed to contributing to lab efficiency and excellence.

**In this position you will **

- Support lab stock management including reagent and supply inventory, ordering and receiving, and preparation of common solutions, with increasing independence as you develop familiarity with lab operations

- Help maintain lab organization and implement process improvements to enhance efficiency and safety

- Perform mammalian and stem cell culture, including cell maintenance, passaging, transfection, virus preparation, differentiation protocols, and co-culture systems, beginning with close guidance and progressing to autonomous execution

- Contribute to molecular biology and genomics workflows, including plasmid construction, PCR, qPCR, gel electrophoresis, DNA/RNA isolation, and sequencing preparation

- Write and update standard operating procedures for lab protocols and processes as you gain expertise

**Requirements **

- Bachelor's degree or equivalent experience in Biology, Molecular Biology, Biochemistry or related field

- 1-2 years of laboratory experience (academic or industry setting)

- Familiarity with standard molecular biology techniques (such as cloning, PCR, qPCR, gel electrophoresis, and DNA/RNA isolation) and mammalian cell culture; hands-on experience preferred but not required.

- Proficiency with basic computer skills, including data entry, spreadsheets, and document preparation.

- Effective organizational, communication, and collaborative skills

The hourly rate for this position is $29.00. This amount does not include benefits or other forms of compensation.

Research Associate I, Konermann Lab

Here at CHLA, we believe every child deserves to enjoy all those special moments that childhood has to offer, free from pain and suffering. This is what inspires our staff to be their best—and they’re equipped with everything they need to succeed. If you want to help create more special moments for children where you’re empowered to deliver the highest quality of care, this is the place to do it.

At CHLA — named best in California for treating children by U.S. News & World Report—we empower our team members to deliver the highest quality care. As a Magnet-designated hospital, we provide compassionate care for our patients more than 528,000 times each year. If you’re ready to make a difference for thousands of children while improving pediatric medicine, join us.

Industry: Hospitals and Health Care
Company Size: 1,001-5,000 employees

Children's Hospital Los Angeles (CHLA)

- This position is Hybrid: flexibility to vary based on research needs.**

**Schedule: ** Monday-Friday, 8:30 AM-5:00 PM

**Purpose Statement/Position Summary: ** The Senior Bioinformatics Scientist will lead the computational analysis of biological data. Will analyze, manage, and interpret experimental results from sequencing, high throughput, spatial, and/or other techniques in order to identify factors that are causal to or associated with genetic disorders or childhood cancers. Will establish workflows and software packages. Will develop customized pipelines, databases and novel methodologies as needed. The Senior Bioinformatics Scientist may have a role in mentoring junior bioinformatics analysts, and may lead various research projects that will result in novel insights and publications. Will also provide research support to investigators and assist in training investigators and new users to use bioinformatics applications and databases.

**Minimum Qualifications/Work Experience: ** PhD degree and 3+ years of related work experience. Or Master’s degree and 5+ years of related work experience.

**Preferred Skills**

- Demonstrated ability to develop and implement complex novel computational methods/algorithms.

- Demonstrated ability to organize and perform analysis of large-scale complex data sets including statistical tests, quality analysis, and machine learning, artificial intelligence, blockchain and or natural language processing.

- Experience with genomic/proteomic data analysis methods.

- Proficiency in various open source and commercially available bioinformatics resources, platforms and software.

- Advanced - expert level linux background and bash scripting experience.

- Expert object-oriented programming experience (C++, R and, or Java) with advanced visualization (HTML5, CSS, Javascript and Shiny).

- Advanced - expert scripting language experience (Perl and Python).

- Advanced - expert database development; structured and unstructured (SQL/MySQL/MongoDB/Redis).

- Familiarity with various publicly available databases such as HGMD, ClinVar, TCGA, ICGC, Ensembl, Refseq, UCSC, 1000 Genome and ExAC.

- Perform variant calling for rare and common variants from whole-genome sequencing data using state-of-the-art genomic analysis pipelines, including DRAGEN.

- Classify and annotate rare variants according to ACMG guidelines to support clinical and research applications.

- Conduct global and local ancestry analyses to enhance variant interpretation and improve diagnostic yield in diverse populations.

- Collaborate with multidisciplinary teams, including geneticists and clinicians, to interpret genomic findings and develop actionable insights.

- Demonstrated ability to manage multiple projects and overlapping deadlines and dependencies.

- Prepare and present research findings in formal reports and at scientific conferences, as well as contribute to peer-reviewed publications.

- Excellent communication skills, both written and verbal.

- Experience in NGS data analysis.

**Education/Licensure/Certification**

**Required: ** Master’s degree in bioinformatics or a related field.

~~**Preferred: ** ~~ PhD degree in bioinformatics or a related field.

Sr. Bioinformatics Scientist

Astrix is the unrivaled market-leader in creating & delivering innovative strategies, solutions, and people to the life science community.  

Through world class people, process, and technology, Astrix works with clients to fundamentally improve business & scientific outcomes across many domains including the laboratory, clinical & regulatory, pharmacovigilance, R&D, and manufacturing. 

Founded by scientists to solve the unique challenges of the life science community, Astrix offers a growing array of strategic, application & platform, data transformation & analytics, change management, and staffing services designed to deliver immediate value to clients and solve their most complex technical and staffing challenges.

Industry: IT Services and IT Consulting
Company Size: 1,001-5,000 employees

Astrix

Pay Rate Low: 60 | Pay Rate High: 64

~~Our client is a patient-driven cardiovascular biotechnology company dedicated to advancing heart disease treatment by developing therapies that address the root causes of disease rather than managing symptoms alone.~~

**Title: **GxP Auditor (Hybrid – South San Francisco, CA)

**Location: ** Hybrid (4 days onsite, South San Francisco, CA)

**Pay rate: ** $60/hr

**Schedule: ** Full-time, M-F 8am-5pm

**Contract-to-hire**

We are seeking a **GxP Auditor ** to join a quality team in a contract-to-hire capacity. This role is ideal for a seasoned auditor with strong GMP experience who is looking to contribute to a growing organization while supporting and helping scale a global audit program.

**Role Overview**

The GxP Auditor will be responsible for executing and supporting audits across internal operations, vendors, and investigator sites, ensuring compliance with global regulatory standards. This individual will also play a key role in strengthening audit program infrastructure, supporting audit reporting, and managing CAPA lifecycle activities.

**Key Responsibilities**

- Plan and conduct GxP audits (primarily GMP), including vendor and clinical/investigator site audits

- Perform audit report reviews and ensure alignment with regulatory and quality standards

- Support the audit lifecycle, including CAPA review, approval, and closure

- Contribute to the development and improvement of audit program infrastructure

- Collaborate cross-functionally with Quality and Operations teams

- Participate in scheduled audits across multiple regions (domestic and some international travel)

- Support upcoming GCP audits and ongoing audit planning activities

- Travel: 20–50%

**Qualifications**

- MUST be a Certified Auditor (required)

- 5–10+ years of experience in Quality, Compliance, or GxP auditing/inspections

- Strong working knowledge of FDA, EMA, ICH, and GMDP regulations

- Hands-on experience conducting GMP audits (vendor and/or clinical site audits preferred)

- Experience reviewing audit reports and managing CAPAs

- Bachelor’s or advanced degree in Life Sciences, Pharmacy, Chemistry, or related field

- Experience in biotech/pharma environments

**Preferred**

- Experience with MHRA and Health Canada regulations

- Familiarity with Veeva and/or Smartsheets

- Strong communication, collaboration, and stakeholder management skills

INDBH

Quality Auditor

UCLA offers a combination that’s rare, especially among public research universities. The breadth, depth and inspired excellence among academic programs—from the visual and performing arts to the humanities, social sciences, STEM disciplines and health sciences—add up to endless opportunity. The location is unmatched: a campus that is unexpectedly picturesque and compact, set in a thriving and diverse global city.

Industry: Higher Education
Company Size: 5,001-10,000 employees

UCLA

**Department Summary**

The caliber of our faculty, staff, and student dentists helps foster a dynamic environment, focused towards the future. Along with our passion and dedication to be among the best in the world, UCLA Dentistry is truly unique. As part of a world-renowned research university, combined with excellent educational programs and clinic training, we believe this is where leaders are made.

**Position Summary**

Under the general and direct supervision of the Project Director and Co-Investigators, the Research Data Analyst will support multiple population and clinical health research projects by conducting statistical analyses, managing datasets, developing reporting systems, and contributing to research documentation. The role emphasizes epidemiologic and biostatistical analysis of longitudinal health data, literature synthesis, data management, and preparation of scientific reports. The individual will support NIH- and foundation-funded research projects focused on HIV, oral health, pediatric and maternal health, and community-based health assessments. Responsibilities include maintaining data systems, ensuring data quality, contributing to analytic plans, preparing summary outputs, and supporting research dissemination.

**Salary & Compensation**

- UCLA provides a full pay range. Actual salary offers consider factors, including budget, prior experience, skills, knowledge, abilities, education, licensure and certifications, and other business considerations. Salary offers at the top of the range are not common. Visit UC Benefit package to discover benefits that start on day one, and UC Total Compensation Estimator to calculate the total compensation value with benefits.

**Qualifications**

- Working knowledge of research functions, including study protocols, data collection, documentation, and reporting requirements. (Required)

- Applied understanding of statistical methods and research design supporting epidemiologic, clinical, and population‑based studies. (Required)

- Demonstrated skills in statistical analysis, data management, database organization, and data quality assurance to support reproducible research. (Required)

- Strong organizational skills and attention to detail, with the ability to follow established research protocols. (Required)

- Excellent written and verbal communication skills. (Required)

- Ability to work both independently on assigned tasks and collaboratively as part of a multidisciplinary team. (Required)

- Commitment to following research integrity standards, reproducibility practices, and laboratory safety protocols. (Required)

- Demonstrated ability to use Tableau, R (or an equivalent statistical and programming software) software, which includes data access, data retrieval, data management, data analysis, and data presentation. (Required)

**Education, Licenses, Certifications & Personal Affiliations**

-  Bachelor's degree in related area and / or equivalent experience / training (Required)

**Special Conditions for Employment**

- Background Check: Continued employment is contingent upon the completion of a satisfactory background investigation.

- Live Scan Background Check: A Live Scan background check must be completed prior to the start of employment.

- Age Requirement: Candidate(s) must be 18 years or older to be eligible to be hired.

- COVID and Flu Vaccinations: The position is subject to providing evidence of inoculation.

- CANRA: The position is designated as a mandatory reporter under CANRA. The employee must sign the "Statement Acknowledging Requirement to Report Child Abuse".

**Schedule**

8:00 a.m. to 5:00 p.m.

**Union/Policy Covered**

RP-Research and Public Service PR

**Complete Position Description**

https://universityofcalifornia.marketpayjobs.com/ShowJob.aspx?EntityID=38&JDName=Research%20Data%20Analyst%202%20RP%20(41233480)

Research Data Analyst 2 RP

Mintz Group is a corporate investigations firm that gathers information before hiring, before transactions, during litigation disputes and after frauds, all over the world.

Clarity in a Complex World

It’s tricky doing business in a complex, cross-border environment. When the truth is complicated and hidden, we find what you need to know to make informed decisions in business relationships, in the workplace and in court. We specialize in one thing: Digging into questions that concern our clients.

► Background Checks that Match Your Real Risks
We’re the only corporate investigations firm that has thought through background checking from A to Z. Literally. Where our competitors make a mystery of what they are checking, we explain each of the 26 steps on our deep menu of due diligence checks. Whether it’s a customized report or one of our best-practice levels, we match background checks to your real risks, providing exactly the due diligence you need. No more. No less.

► Litigation Investigations and Litigation Support
We help litigators - across all practice areas - find admissible evidence hidden along obscure paper trails and in the memories of apprehensive witnesses. Many of our investigations end with the tracing and recovery of opponents' assets.

► Fraud Investigations
Mintz Group conducts a variety of investigations on behalf of clients who believe they have been victims of fraud. And we regularly assist counsel with anti-corruption (FCPA, etc.) investigations.

Subscribe to our newsletter here: https://mintzgroup.com/subscribe/

Industry: Security and Investigations
Company Size: 201-500 employees

Mintz Group

**Managing Investigator ****Discover Mintz Group**

At Mintz Group, we specialize in uncovering the truth. For over 30 years, we have provided top-tier investigative services to help our clients make informed decisions, mitigate risks, and seize opportunities. Our services span executive due diligence, transaction due diligence and litigation support for dispute resolution, conducted by a dedicated team of over 250 investigators across 12 offices worldwide.

Why Join Us?

-  Global Impact: Work with a firm that conducts over 10,000 investigations annually in more than 130 countries, making a significant impact on a global scale.

-  Expert Team: Join a team of professionals who are leaders in the field, bringing together diverse expertise across industries.

-  Growth Opportunities: Be part of a dynamic environment that offers continuous learning and career advancement opportunities.

-  Innovative Culture: Thrive in a culture that encourages innovation, excellence, and collaboration, ensuring that we stay ahead in the industry.

Be part of a firm that is dedicated to delivering factual, reliable, and actionable intelligence, contributing to the success and security of our clients.

What’s This Job Is About?

We’re seeking a Managing Investigator to join our Executive Due Diligence team. This critical role has two components: individual contributor and case manager. As an individual contributor, you will conduct sophisticated research on complex or high-profile cases, using advanced investigative skills. As a case manager, you will focus on managing routine cases that involve in-depth research, and providing analysis and data synthesis in client-ready deliverables. You will collaborate closely with other case managers as well as leadership across various practice groups, including Executive Due Diligence, Transaction Due Diligence and Disputes. Through your meticulous attention to detail and oversight of the entire investigative process, you will deliver polished, accurate, actionable intelligence that strengthens the Mintz Group’s reputation for excellence and supports our strategic goals.

What are Your Key Responsibilities?

**Conduct Complex Investigations**

-  Handle cases with higher complexity and profile, requiring advanced investigative skills and discretion.

-  Conduct in-depth database searches and analyze nuanced legal, corporate, and public records.

-  Compile and synthesize significant amounts of data into insightful and professionally written client reports, often for high-stakes situations

**Enhance Expertise And Mentor Junior Team Members**

-  Continue professional development through advanced training programs and by taking on challenging cases.

-  Act as a resource for junior investigators by sharing knowledge and offering guidance.

-  Support team dynamics by contributing to collaborative problem-solving sessions and knowledge-sharing initiatives.

**Optimize And Innovate Investigative Practices**

-  Develop and refine investigative methodologies to tackle complex cases more efficiently.

-  Demonstrate critical thinking and advanced pattern recognition to identify subtle connections and enhance case outcomes.

-  Champion initiatives to integrate new tools or processes that improve research accuracy and reduce turnaround times.

**Uphold Quality And Precision In Deliverables**

Ensure every investigation adheres to the highest standards of accuracy, thoroughness, and professionalism.

Conduct rigorous reviews of all deliverables, leaving no detail unchecked, to provide clients with comprehensive, actionable insights.

Maintain a commitment to confidentiality and integrity in handling sensitive information.

**What Makes You a Great Fit**

-  Experience: 4-7 years of relevant work experience in investigations, risk advisory, or due diligence. Experience in client-facing professional services preferred.

-  Research Expertise: Proficient in using investigative databases such as Westlaw and Nexis, with demonstrated ability to analyze legal, corporate, and other public records.

-  Writing Skills: Exceptional ability to draft clear, concise, and comprehensive investigative reports tailored to client needs.

-  Attention to Detail: Proven track record of delivering high-quality, error-free work, adhering to firm guidelines, and conducting exhaustive reviews.

-  Analytical Thinking: Strong capacity to distill large amounts of complex information into actionable conclusions while identifying patterns and anomalies.

-  Tech Savvy: Familiarity with investigative tools and platforms, and ability to quickly learn and adapt to new technologies.

-  Global Perspective: Multilingual capabilities are a plus, contributing to a broader understanding of cross-border investigations and diverse client needs.

-  Educational Background: A bachelor’s degree is required; an advanced degree is preferred.

-  Adaptability: Demonstrated ability to manage multiple projects simultaneously, meet deadlines, and pivot effectively in response to shifting priorities.

Ready to Join Us?

Our ideal candidate will have expertly navigated the complexities of investigative research, synthesizing large volumes of information into actionable insights while ensuring accuracy and clarity. Leading applicants will excel in analytical thinking, time management, and collaborating with a range of team members – including junior investigators, fellow case managers, and practice leadership – to meet client objectives.

To thrive in this role, the successful candidate will focus on hands-on investigative activities, leveraging data-driven tools and methods while relying on critical thinking and attention to detail to deliver high-quality results.

This role involves a hybrid work setup candidates are required to live in Washington, DC, San Francisco, CA, or Denver, CO

**Why You'll Love Working With Us**

-  Competitive Salary: $90,000- 105,000

-  Discretionary Bonus

-  Flexible Time Off-Policy

-  Health Benefits: Comprehensive medical, dental, and vision coverage

-  Retirement Savings: 401k plan with employer match

-  Parental Leave

-  Hybrid working environment: Candidate must live in San Francisco, CA

-  Life Insurance: Company-sponsored basic life and AD&D insurance

-  Additional Benefits: Flexible spending accounts (FSAs), Transit and Parking

**Our Commitments As An Employer**

Mintz Group is committed to providing equal employment opportunities to all individuals. We do not discriminate against any applicant or employee based on gender, transgender status, race, color, religion, marital status, pregnancy, national or ethnic origin, ancestry, citizenship, sexual orientation, age, veteran status, genetic information, mental or physical disability (unless such disability is a bona fide occupational qualification), gender identity or expression, or any other characteristic protected by federal, state, or local law. Our policy of equal employment opportunity applies to all aspects of the employment relationship, including recruitment, hiring, promotion, transfer, training opportunities, termination, wage and salary administration, and the application of benefit plans and company policies.

Managing Investigator - Executive Due Diligence

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