169 Results for

Senior Research Jobs in El Monte, CA

Jobs

Marina del Rey, CA14 days ago

$82,705.68–$133,068.24 Per Year

The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities. Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.

Santa Monica, CA30+ days ago

$82,705.68–$133,068.24 Per Year

New!

El Segundo, CA4 days ago

p>ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells.

Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support.

Los Angeles, CA30+ days ago

$145,000–$175,000 Per Year

The Senior Contract Oncology Clinical Research Associate (SCRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization.

Responsibilities for the Senior Contract Oncology Clinical Research Associate:

Conduct site and study visits and perform all site monitoring activities across multiple study.

Marina del Rey, CA13 days ago

$82,705.68–$133,068.24 Per Year

Los Angeles, CA30+ days ago

$68,920.14–$110,890.02 Per Year

This role is well-suited for an experienced research professional who can lead study activities, manage priorities, and ensure high-quality, compliant execution across complex research projects. The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up through closeout.

Los Angeles, CA30+ days ago

$6,892.14–$11,089.02 Per Year

This role is well-suited for an experienced research professional who can lead study activities, manage priorities, and ensure high-quality, compliant execution across complex research projects. Key Responsibilities: Manage day-to-day operations for one or more clinical research studies, including multicenter and investigator-initiated trials.

CA30+ days ago

$113,300–$169,900 Per Year

p>Preferred Experience/Education/Skills:

Typically requires a minimum of 5 years of related experience with a bachelors degree, or 3 years of relevant experience with a masters degree, in Bioinformatics, Clinical data analysis, Molecular Biology, Genetics, or Biochemistry.
Work closely with other sales team members, including account managers and other sales specialists to make customers successful in genomic data analysis and interpretation.

Sherman Oaks, CA30+ days ago

As a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role.

New!

Santa Monica, CA1 day ago

$93,927.51–$151,099.73 Per Year

The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities. + Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.

Los Angeles, CA30+ days ago

Remote

$140,000–$165,000 Per Year

ul>

Conducts all activities involved in on-site visits consistent with the applicable Clinical Monitoring Plan (CMP), SOPs, and ICH GCP for site qualification, site initiation, interim monitoring, site close-out, and other site visits (eg, booster visits). The physical demands of the home office are normally associated with extended amounts of time sitting and using office equipment (including a computer, keyboard, and mouse), standing, walking, sitting, speaking, and hearing.

Irvine, CA9 days ago

$105,500–$168,800 Per Year

For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Tustin, CA15 days ago

$84,000–$105,000 Per Year

Research Associate, you'll have the opportunity to focus on developing Cell-based, ELISA, HPLC, CE, PCR and/or SDS-PAGE methods, and you'll work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.

Sylmar, CA30+ days ago

$90,000–$180,000 Per Year

Whether it's glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Demonstrated ability to manage multiple complex projects simultaneously, prioritize effectively, and deliver high‑quality scientific work under tight timelines, with strong attention to detail and commitment to analytical rigor.

CA15 days ago

Remote

$131,000–$150,000 Per Year

p>This position could act as the leading CRA for the CRA team, and will assist COPM in all projects set up and management aspects and require a proven record of hands-on experience in processes such as study feasibility and site qualification, TMF and ISF set up, creation of monitoring plans and preparation of IRB submission packages among other duties.

Ensure the detection and careful monitoring of adverse events (AE) and serious adverse events (SAE) representing pharmacovigilance cases and ensure the transmission of information to the departments concerned; 4. Manage the logistics of the investigative site(s) including investigational products, clinical materials and biological samples.

CA17 days ago

p>Advance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first!

Experience monitoring complex Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred.

CA21 days ago

$31.83–$63.65 Per Hour

p>Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle''s differing products, industries and lines of business. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_mb@oracle.com or by calling 1-888-404-2494 in the United States.

CA30+ days ago

p>Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks.

Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.

Long Beach, CA24 days ago

$110,520–$138,150 Per Year

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

New!

Duarte, CA3 days ago

li>5+ years progressively responsible for business management, project and program management within an academic or research environment including experience in research budget development and management plus 3 years of experience in management capacity. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

Los Angeles, California16 days ago

li>

Willing and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, near major HUB airports to support efficient regional travel.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Los Angeles, CA29 days ago

Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to:

Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.

Pasadena, CA9 days ago

The successful candidate will push forward multiple rodent in vivo projects by serving as a surgical expert, contributing to daily laboratory operations and experimental design, assisting with in vitro experimental workflows, and helping maintain shared research facilities.

The Senior Research Associate will be an integral member of the laboratory alongside the lab manager, technicians, postdoctoral fellows, and graduate students to ensure efficient laboratory operations and contribute to ongoing research projects.

Los Angeles, CA30+ days ago

li>

Use open-source scientific computing packages like Stim, Qiskit, NumPy, Networkx, Scipy, Scikit-learn, and PyTorch to build high-quality research code to develop, demonstrate, and test new algorithms and methods. We push toward quantum advantage by developing cutting-edge applications, employing AI, control theory, and physics principles to optimize and automate critical parts of the quantum computing stack.

CA30+ days ago

$82,000–$103,000 Per Year

p>Position Summary:

The Senior Research Associate, Drug Product Development, will support the development of drug product formulations from early preclinical enabling studies through clinical supply for First-in-Human (FIH) trials. The position works closely with formulation scientists, analytical, DMPK, toxicology, and manufacturing teams to deliver high quality drug products in a fast-paced development environment.

Los Angeles, CA17 days ago

Remote

$120,000–$130,000 Per Year

ul>

Expertise in using computer-based research tools: Lexis, Westlaw, Bloomberg Law, Intelligize, Practical Law, PLI, Capital IQ, Deal Point Data, SNL, VitalLaw, Pitchbook, Courthouse News Services, Accurint, HeinOnline, Fromcounsel, Filings Expert and more.

Works independently and with the Knowledge Strategy (KS) team and selected practice areas to choose, collect, organize, maintain, and update content for practice area websites and databases.

CA17 days ago

Remote

$97,000–$193,000 Per Year

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

Los Angeles, CA30+ days ago

p>The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians.

The Senior Regulatory Coordinator prepares and submits moderately complex protocols and supporting documentation to regulatory bodies and research committees involved in the pre-award and post-award process.

Pomona, CA24 days ago

$156,100–$190,700 Per Year

Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.

Pomona, California23 days ago

Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs.

Los Angeles, California16 days ago

p>The Clinical Research Assistant (CRA) is an entry-level, pre-professional role designed for pre-medical or health-sciences students seeking structured exposure to clinical research and patient-facing clinical environments.

This role does not include independent study coordination or regulatory decision-making responsibilities and functions under close supervision at all times.

Los Angeles, California21 days ago

ul>

Works independently and with the Knowledge Strategy (KS) team and selected practice areas to choose, collect, organize, maintain, and update content for practice area websites and databases.

Los Angeles, CA30+ days ago

$76,675.67–$90,000 Per Year

p>If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser: https://wd5.myworkday.com/usc/d/inst/1$9925/9925$141409.htm.

The successful candidate is expected to be based in the greater Los Angeles area (encompassing Los Angeles, Orange, San Bernardino, Riverside, and Ventura county; within daily commute distance from campus), but some level of working from home is possible.

Hawthorne, California16 days ago

Such activities may include data analysis, model development and other related technical activities, developing general R&D software tools to increase company capabilities, and documenting work in appropriate company and customer reports.

Systems Technology Inc. (STI) is a private, employee-owned company (ESOP) that provides engineering consulting and product development with a focus on safety.

Los Angeles, CA30+ days ago

$27.08–$43.55 Per Hour

p>The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities.

Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.

New!

Los Angeles, CA1 day ago

$74,445–$152,460 Per Year

Strong writing skills in a variety of styles to draft persuasive text for a variety of audiences while ensuring adherence to funding sponsor's guidelines. You will be expected to manage larger, more complex PI portfolios as well as help oversee, train, and mentor junior research administrators' trainees.

Los Angeles, CA30+ days ago

$29.28–$47.10 Per Hour

The Department of Medicine, Division of Gastroenterology is seeking to hire an Assistant Clinical Research Coordinator to support the successful execution of clinical research studies and trials. As a condition of employment, the final candidate who accepts an 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; or have filed an appeal of a finding of substantiated misconduct with a previous employer.n.

Los Angeles, CA30+ days ago

Our lawyers work at the intersection of government, technology and business, and we remain committed to our guiding principles of providing quality, excellent legal and client services; developing diversity among our lawyers and staff and cultivating an environment that promotes an ambitious spirit, collaboration and collegiality by drawing on the extraordinary talents and dynamic experience of our lawyers.

Deliver complex, high‑stakes legal and business research for attorneys and senior firm leadership using a wide range of digital and print resources; bill research time to client matters as appropriate.

Los Angeles, CA30+ days ago

$98,640–$123,300

What You Will Be Doing

Deliver timely, high quality legal and business research to attorneys and senior stakeholders across the firm; bill research time to client matters as appropriate.

Irvine, CA30+ days ago

p>The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

Los Angeles, California30+ days ago

p style="min-height:1.5em">The ideal candidate will possess extensive experience in strategic market research (both quantitative and qualitative methodologies) and managing a portfolio of clients, effective organizational skills, the ability to delegate tasks efficiently, a keen attention to detail, and a commitment to delivering accurate and comprehensive market insights.

As a Senior Market Research Manager, you will lead a diverse range of quantitative and qualitative research projects, serving as the primary point of contact, and managing the complete execution of projects that address the major business questions for our Fortune 500 clients across a variety of industries.

Los Angeles, CA13 days ago

$27.08–$43.55 Per Hour

The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.

New!

Santa Monica, CA1 day ago

$30.74–$49.46 Per Hour

The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. + Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.

Los Angeles, CA30+ days ago

$29.28–$47.10 Per Hour

Orange, California30+ days ago

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

*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.

Culver City, CA30+ days ago
$75,000–$100,000 Per Year
li>
Drive successful project execution, collaborating with senior team members and providing input and oversight to junior team members on quality control processes at each step of the research lifecycle, from checking survey programming logic, questionnaire proofing, number checking and proofing reports and presentations for accuracy. Youll manage end-to-end research initiatives, from crafting surveys and discussion guides to transforming data into compelling narratives that address key strategic questions -primarily focused on Film and TV content and marketing.

CA17 days ago
$85,000–$100,000 Per Year
li>Data analysis techniques and software - Strong experience with interpreting advanced data techniques such as statistical significance testing, correlation analysis, maxdiff, TURF, key drivers analysis, multivariate analysis techniques (such as cluster/segmentation analysis), conjoint, and discrete choice analysis.
Partner with internal and external operations teams (programming, fieldwork, facilities, moderators, data processing) to drive projects forward on stringent timelines.

Los Angeles, CA30+ days ago
$82,105.68–$133,068.24 Per Year
p>Required • Bachelors Degree or three-to seven years of study coordination or clinical research coordination experience • Ability to work efficiently and complete tasks with a high degree of accuracy • Ability to organize multiple projects for efficiency and cost-effectiveness • Analytical skills sufficient to work and solve problems • Ability to work flexible hours to accommodate research deadlines • Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines • Ability to be flexible in handling work delegated by more than one individual or in the course of delegating work • Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership • Strong written communication skills, ability to compose advanced correspondence and manage large file systems • Advanced typing and computer skillability, including word-processing, use of spreadsheets, email, and data entry • Ability to handle confidential material with judgment and discretion • Skill in managing diverse, complex tasks and information transfer among multiple constituents • Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets • Advance knowledge of the clinical research regulatory framework and institutional requirements • Ability to supervise and delegate clerical work as needed • Advanced knowledge of Good Clinical Practice (GCP) for clinical research. The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies, which may include multicenter clinical trials, both NIH and industry-sponsored, local investigator-initiated clinical trials, and/or programmatic clinical research activities.

New!
Los Angeles, CA1 day ago
$30.74–$49.46 Per Hour
The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. + Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.

Los Angeles, CA30+ days ago
$82,705.68–$133,068.24 Per Year
p>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 ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities.

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Senior Research Jobs in El Monte, CA

Senior Clinical Research Coordinator - HematologyOncology Marina del Rey UCLA Health System

Senior Clinical Research Coordinator - HematologyOncology Santa Monica UCLA Health System

Senior Clinical Research Associate, Field Monitor ImmunityBio Inc

Senior Oncology Clinical Research Associate Zp Group Llc

Senior Clinical Research Coordinator - Hematology/Oncology (Marina del Rey) University of California

Sr. Clinical Research Coordinator - Radiation Oncology UCLA Health System

Sr. Clinical Research Coordinator - Radiation Oncology University of California

Senior Research Informatics Sales Specialist, Pacific Illumina Inc

Senior Clinical Research Associate ICON Plc

Senior Clinical Research Coordinator - Hematology/Oncology (Santa Monica) UCLA Health

Senior Clinical Research Associate - Remote Position Puma Biotechnology Inc

Senior Specialist, Clinical Research Becton Dickinson and Co

Sr. Research Associate, Analytical Development Avid Bioservices Inc

Senior Clinical Research Scientist Abbott Laboratories

Sr. Clinical Research Associate Les Laboratoires Servier SAS

Senior Clinical Research Associate PSI CRO AG

Oracle Life Sciences Sr. Research Consultant- Epidemiology/Oncology Oracle Corp

Senior Clinical Research Associate - Oncology - West Coast - FSP Parexel International Corp

Sr. Clinical Research Associate ICON Plc

Senior Manager, Administrative Clinical Research Programs City of Hope

Senior Clinical Research Associate IRE

Senior Research Science Liaison Syneos Health Inc

Senior Research Associate California Institute of Technology

Senior Research Scientist, Quantum Error Correction Q-CTRL Pty Ltd

Sr. Research Associate, Drug Product Development Crinetics Pharmaceuticals Inc

Senior Research & Knowledge Analyst Northern California Association of Law Libraries

Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote Worldwide Clinical Trials Holdings Inc

Senior Regulatory Coordinator - The Angeles Clinic & Research Institute Cedars-Sinai Medical Center

Sr. Research Scientist Envista Holdings Corp

Sr. Research Scientist Envista Dentistry

Clinical Research Assistant (Pre-Medical Track) Must Speak English and Spanish Angel City VA

Senior Research & Knowledge Analyst Skadden

Senior Research Associate University of Southern California

Senior Research Engineer STI

Assistant Clinical Research Coordinator - HematologyOncology UCLA Health System

Senior Research Administrator - Department of Medicine UCLA Health

Assistant Clinical Research Coordinator UCLA Health System

Senior Research Analyst (2365-437) Wilmer Cutler Pickering Hale and Dorr LLP

Senior Research Analyst WilmerHale

Sr. Clinical Research Director (CRDN) Medtronic Plc

Senior Research Manager (Ongoing Recruitment) Fuel Cycle

Assistant Clinical Research Coordinator - Hematology/Oncology University of California

Research Assistant - Hematology/Oncology (Santa Monica) UCLA Health

Assistant Clinical Research Coordinator University of California

SR. CLINICAL RESEARCH COORDINATOR - HYBRID University of California, Irvine

Entertainment Market Research Manager / Senior Manager National Research Group Inc

Senior Market Research Manager, Technology Clients National Research Group Inc

Senior Clinical Research Coordinator - Department of Medicine - Office of Research Administration UCLA Health System

Assistant Clinical Research Coordinator - Hematology/Oncology UCLA Health

Senior Clinical Research Coordinator - Department of Medicine - Office of Research Administration University of California

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