61 Results for

Research Jobs in Laguna Woods, CA

Jobs

New!

Corona, CA4 days ago

$26–$29 Per Hour

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. A prominent oncology network has a Riverside clinic that is seeking a polished, patient-first Non-Clinical Medical Assistant/Office Supervisor to own the front-office experience and keep daily operations running smoothly.

New!

Newport Beach, CA2 days ago

$52–$75

Job OverviewWe are actively seeking a Clinical Research Coordinator RN II to join a leading healthcare organization at Hoag. This is an excellent opportunity for an experienced RN with a background in clinical research, especially in advanced therapies such as cell therapy and CAR-T.

Irvine, CA10 days ago

$30–$35 Per Hour

Coordinate with cross-functional teams including Clinical, Supply Chain, Manufacturing, Finance, and Quality . If you think this Clinical Operations Specialist position is a good fit for you, please reach out to me - feel free to call, e-mail, or apply to this posting!

Irvine, CA10 days ago

By opening the new hospital – City of Hope’s second academic hospital in California – we are fulfilling our promise to Orange County and completing the continuum of care for people with cancer. Seeking research and mission-minded physicians who provide exceptional patient-centered care through clear communication and collaboration with members of the subspecialty teams.

New!

Irvine, CA2 days ago

$30–$35 Per Hour

Identify, develop, recommend, and implement process development and improvement solutions to optimize global trial workflow. Produce daily/weekly/monthly reports as well as ad hoc requests to be fulfilled by the operations team.

Orange, California30+ days ago

Proven organizational skills and attention to detail; ability to multi-task, prioritize a complex and dynamic workload, meet rigid deadlines despite interruptions, frequent workload changes and competing demands, and achieve high productivity/quality within short time frames; skill in working independently, taking initiative and following through on assignments and ability to work as part of a team. *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.

Newport Beach, CA30 days ago

Contractor

Job Title: Registered Nurse (RN) - Clinical Research Coordinator II Job Location: Newport Beach, CA Job Duration: 2-3 Months (possibility of extension) Job Summary: The Clinical Research Coordinator-Registered Nurse II (CRC RN-II) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors. Job Responsibilities: Manages complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies.

Huntington Beach, CA30+ days ago

$19–$33 Per Hour

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Assistantis an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.

Whittier, CA30+ days ago

$27.44–$45.27

The fully integrated network is comprised of PIH Health Downey Hospital, PIH Health Good Samaritan Hospital, PIH Health Whittier Hospital, 37 outpatient medical office buildings, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, digestive health, orthopedics, women’s health, urgent care and emergency services. The organization is nationally recognized for excellence in patient care and patient experience, and the College of Healthcare Information Management Executives (CHIME) has identified PIH Health as one of the nation’s top hospital systems for best practices, cutting-edge advancements, quality of care and healthcare technology.

Irvine, California29 days ago

Listed among America’s Best Hospitals by U.S. News & World Report for 23 consecutive years, UCI Medical Center provides tertiary and quaternary care and is home to Orange County’s only National Cancer Institute-designated comprehensive cancer center, high-risk perinatal/neonatal program and American College of Surgeons-verified Level I adult and Level II pediatric trauma center, gold level 1 geriatric emergency department and regional burn center. *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.

Oceanside, California14 days ago

£81,402–£101,755

Develop skills in data analysis and interpreting experiment outcomes including the ability to evaluate data quality and recognize anomalous results. · Recommend alternatives, research new methods and techniques and proactively seek out senior personnel to discuss potential solutions to problems.

Irvine, California24 days ago

$25–$25 Per Hour

Conduct basic vetting of accounts to determine whether the business sells supplements, appears to offer private label products, carries competitive brands, and the general size or profile of the store. Prior experience in research, data entry, lead generation, administrative support, sales support, or account/prospect research preferred.

New!

Newport Beach, CA1 day ago

The CRC RN-II is involved in all aspects of research studies from protocol review, preparation and administration of the informed consent, subject recruitment, accurate data collection and completion of case report forms (CRFs), adverse event reporting, and scheduled subject follow-up and maintenance of regulatory binders. The CRC RN-II is responsible for managing complex clinical research trials including drug/device/biologic studies that may involve industry-sponsored Phase I, II, III and IV clinical trials, government funded clinical research and investigator initiated clinical research.

Orange, California14 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.

Irvine, CA30+ days ago

Full-time

Purpose: The Associate Director, Clinical Science & External Research (CSER) will drive end-to-end evidence generation and dissemination strategies (EGS/EDS) of scientific findings from clinical trials and postmarket studies sponsored by Johnson & Johnson MedTech Electrophysiology to generate clinical evidence for the company's pipeline that impacts patient lives. The ideal candidate for this position has proven success in the development of scientific communications and evidence dissemination plans in a medical device or related industry, is versed in supervising personnel writing and editing manuscripts, is knowledgeable of the cardiac arrhythmia medical device industry, and is familiar with pertinent regulations and guidelines governing clinical trial execution and clinical data publication.

Newport Beach, CA30+ days ago

The Clinical Research Coordinator-Registered Nurse II (CRC RN-II) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors. Excellent verbal and written communications and presentation skills; excellent organizational skills; close attention to detail and excellent interpersonal skills to work effectively in a diverse team.

Irvine, California30+ days ago

Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. The University of California, Irvine School of Education is a diverse, dynamic and collaborative community focused on advancing education sciences and contributing to improved education opportunities and outcomes for individuals across the education lifespan, from early childhood to higher education and beyond.

Huntington Beach, CA30+ days ago

$55,000–$85,000 Per Year

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

Whitter, CA30+ days ago

$52.50–$84.25

The clinical trial nurse is required to have comprehensive knowledge in all areas of protocol design, strong clinical assessment and decision-making skills, ability to navigate fast-paced hospital environments, manage multiple studies, excellent communication and patient education abilities, knowledge of federal regulations (FDA, OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). The fully integrated network is comprised of PIH Health Hospital - Whittier, PIH Health Hospital - Downey and PIH Health Good Samaritan Hospital, 27 outpatient medical locations, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, women’s health, urgent care and emergency services.

Orange, California28 days ago

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. Responsibilities: Under the general direction of the Assistant Director of Clinical Research Operations of the UCI Center for Clinical Research (CCR), the Clinical Research Manager (CRM) is responsible for all clinical research operational matters in fulfilling the mission of CCR under the University of California Irvine School of Medicine and the overall UC Irvine Health enterprise.

Irvine, California15 days ago

Additionally, the incumbent is responsible for leading on-going training and education of CRCs, leading and managing pre-study site selection visits (PSSVs) including liaising with all appropriate ancilliary units (e.g., Investigational Drug Service, Pathology, Radiology, etc.) for the conduct of the trial, managing quality assurance and quality improvement goals and objectives through routine audit reviews of the team’s portfolio. The incumbent is also responsible for maintaining communication with all elements of a multi-level and multi-discipinary 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.

Orange, California14 days ago

$27.40–$34.43 Per Hour

The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and . In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI).

Irvine, California30+ days ago

Irvine, CA30+ days ago

$30–$40 Per Hour

As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs).

Irvine, California8 days ago

Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. The Clinical Research Navigator works in close collaboration with Principal Investigators (PIs), Clinical Research Coordinators (CRCs), and other research support services to promote compliant and streamlined trial execution.

Vista, CA13 days ago

$31–$35 Per Hour

DESCRIPTION: The Research Assistant I assists with the development of new assays for diagnostics and research projects, through various phases of inception, planning and transfer to the clinical lab. Collaborate with other members of the scientific staff within and outside the R&D group, including academic collaborators, external consultants, and scientists.

Irvine, California25 days ago

$35.77–$36.54 Per Hour

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. Clinical research offices and clinics are located at the UCI Medical Center in Orange and the UCI campus in Irvine, as well as various clinics at community sites throughout Orange County.

Irvine, CA30+ days ago

$100,000–$160,000
Full-time

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Draft legal documents including trust agreements, operating agreements, asset protection structures, promissory notes, and entity formation documents.

Oceanside, CA14 days ago

$35–$39.56 Per Hour
Contractor

Ability to collaborate with Technical Operations during technology transfer from process development to GMP manufacturing, including serving as a process development representative during purification operations, providing technical troubleshooting and identifying opportunities for future process and equipment improvements. Ability to work effectively within the purification team to help design and execute experiments supporting process definition, optimization, and characterization with an increasing level of independence.

Murrieta, CA9 days ago

Full-time

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.

Orange, California14 days ago

Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors.

Riverside, CALIFORNIA30+ days ago

Remote

You will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.

Lake Elsinore, CA30+ days ago

Remote

The hiring company conducting the research will rely heavily on employee / contractor participation and feedback in order to make critical business decisions in areas including but not limited to marketing and product development. We expect you to show up on time, listen to and follow instructions carefully and complete each assignment taken.

Oceanside, CA30+ days ago

$74,979–$93,724 Per Year

Perform cell-based reporter assay and flow cytometry analysis to support late-stage . · Experience with analytical methods such as ELISA, cell binding assay, or reporter assay.

Oceanside, CA30+ days ago

$68,773–$85,973 Per Year

Monitor and evaluate purification process performance data, report and present findings, and proactively seek out senior personnel to discuss potential solutions to problem. BS/BE degree Chemical/Biochemical Engineering, Biochemistry, Biology, or a related scientific .

Orange, CA30+ days ago

Full-time

Talley Law Group (TLG) and its affiliated entity Talley LLP (Talley) deliver integrated tax, legal, accounting and consulting services to entrepreneurially driven businesses and high-net-worth individuals. This is a client-facing, advisory-driven role for an attorney who thrives on building relationships, solving complex individual tax challenges, and bringing in new clients within the high-net-worth space.

New!

Oceanside, CA1 day ago

Oceanside, CA15 days ago

Oceanside, CA14 days ago

$35–$39.50 Per Hour
Contractor

Key Responsibilities: Design and execute experiments supporting downstream process development (DSP) Perform protein purification using: AKTA chromatography systems Tangential Flow Filtration (TFF) / UF/DF Harvest centrifugation and filtration Apply Design of Experiments (DOE) for process optimization Support scale-up activities from bench to pilot and manufacturing scale Develop scale-down models and assess process robustness Analyze and interpret data; identify trends and process improvements Collaborate with cross-functional teams (MSAT, Manufacturing, Analytical, QA) Support technology transfer to GMP manufacturing Assist in process characterization, validation, and documentation Present findings and contribute to team discussions Key Requirements and Technology Experience: BS degree + 2+ years of relevant experience OR MS degree + 0+ years of relevant experience Degree in Biochemistry, Chemical/Biochemical Engineering, Chemistry, or related field Hands-on experience in downstream process development (NOT upstream) Strong experience with: AKTA chromatography systems UF/DF or Tangential Flow Filtration (TFF) Chromatography (Protein A, IEX, HIC preferred) Experience with: Process scale-up (bench pilot manufacturing) Scale-down models and process robustness Design of Experiments (DOE) Experience with Antibody Drug Conjugates (ADC) Knowledge of cGMP and technology transfer Experience in biologics (mAbs, bispecifics, fusion proteins) Familiarity with analytical methods (SEC/HPLC, CE, HCP) Our client is a leading Healthcare Industry and we are currently interviewing to fill this and other similar contract positions. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners.

Irvine, California30+ days ago

Seal Beach, CA30+ days ago

$20–$30 Per Hour

A data-driven, integrated marketing agency, we develop meaningful, culturally-relevant marketing communications programs that drive measurable results. The offered salary or hourly rate is based on several factors, including, but not limited to, overall experience, relevant experience, education level, certifications, applicable skills and expertise, and location of the position.

Irvine, CA30+ days ago

$124,000–$335,000 Per Year

You are expected to leverage your specialized knowledge and technical acumen of industry-leading business trends, the firm’s client service offerings, and professional industry networks to deliver quality results to clients and provide strategic input into the firm’s business strategies. Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: + Craft and convey clear, impactful and engaging messages that tell a holistic story.

New!

Irvine, CAToday

$100,000–$200,000 Per Year

The ideal candidate will have hands-on experience creating QC systems for, developing, validating, and troubleshooting immunoassays for clinical or research applications, with a strong understanding of assay performance characteristics, reagent development, and analytical methods. The selected candidate will be responsible for: Design, develop, optimize, and validate immunoassays for automated platforms including Phadia and/or IMMULITE systems.

Irvine, CA30+ days ago

Key Responsibilities: • Support and organize the preparation of Clinical Study binders • Supervision of clinical study applications/submissions to Ethical Committees and Competent Authorities as an administrative support function to the Study Managers; • Support the Study Managers upon request from study managers based on project needs; • Responsible for all document archiving; • Control document validity and compliance (i.e. insurance certificates, etc.); • Organization of meetings related to clinical investigations such as Clinical Event Committees, Data Safety Monitoring Boards, Executive Committees and Steering Committees; • CTMS support • Support clinical department on all business needs • Organize and document (paper and LMS) together with Clinical Managers/Directors employees trainings and all internal meetings; • Manage all administrative aspects related to the Clinical Programs Europe THV in term of clinical study cost accountability; • Conduct payment overviews (cost lists and invoices) and issue payments upon request • Conduct periodic audits of documentation and may participate in internal master file audits • Provide coaching and training to lower level employees • Interact with clinical sites to resolve more complex device accountability issues • Provide training and technical support for internal and external users and set-up of new users in Wavemark • Strict attention to detail • Ability to interact professionally with all organizational levelsEducation:Education and Experience: H.S. Diploma or equivalent 6 years experience previous related experience Required Additional Skills: • Proven expertise in MS Office Suite, Adobe, and ability to operate general office machinery • Experience with an ERP software, JDE and CTMS (Clinical Trial Management System) preferred • Excellent written and verbal communication skills and interpersonal relationship skills • Ability to work in a fast paced environment • Demonstrated problem-solving and critical thinking skills.

Tustin, CA30+ days ago

Actual compensation details will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. Recognized as a Top Workplace by the Orange County Register in 2021, 2022, and named a Top Workplace USA in 2023, Zymo Research continues to be a vibrant community where employees thrive, feel connected, and are inspired by their work.

Newport Beach, California29 days ago

$120,000–$140,000 Per Year

Candidate Profile: In addition to a strong work ethic and motivation to learn, the Senior Associate position requires the following skills: strong financial modeling, valuation skills and research skills, meticulous attention to detail, developing communication (both written and verbal) skills, a high level of organization, creativity, intellectual curiosity, resourcefulness, and an ability to work independently and multi-task. Position Overview: Green Street seeks ambitious, motivated candidates with a passion for the markets and a desire to build a career at the confluence of equity analysis and real estate research.

Cypress, CA30+ days ago

Full-time

Answers questions from vendors and develops new evaluation/testing approaches as needed to achieve internal combustion engine (ICE), hybrid electric vehicle (HEV), and battery electric vehicle (BEV) performance targets. Defines the best practices in North American market to develop competitive future products with higher efficiency, longer range, easier/faster charging, higher safety, and lower production costs.

Newport Beach, CA30+ days ago

Full-time

Aristotle Capital Management, LLC, Aristotle Credit Partners, LLC, Aristotle Capital Boston, LLC, Aristotle Atlantic Partners, LLC, Aristotle Pacific Capital, LLC, and Aristotle Investment Services, LLC, are affiliated organizations. Actual compensation will be dependent on factors, including but not limited to, the individual’s qualifications, relevant experience, knowledge, skills, education, internal equity, and physical work location within the state.

Anaheim, CA30+ days ago

Remote

$15,000–$36,000

We’re inviting individuals from all backgrounds, including those searching for entry level positions, such as, receptionist or typist roles, to express interest in joining upcoming consumer research studies. Research formats vary and may include focus groups (remote online or in-person), video interviews, product evaluations, or digital feedback sessions .

Irvine, CA30 days ago

Full-time
Employee

8 years of experience developing machine learning algorithms specifically for audio applications (e.g., neural noise suppression, acoustic modeling, or speech enhancement). Lead algorithm feasibility research for "moonshot" audio initiatives—specifically Superhuman Hearing—operating outside the gravitational pull of immediate product timelines.

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Research Jobs in Laguna Woods, CA

Jobs

Office Supervisor (Medical Assistant)Jobot

Travel Nurse RN - Clinical Nurse Coordinator - $52 to $75 per hour in Newport Beach, CATravelNurseSource

Clinical Operations Specialist {169462}A-Line Staffing Solutions LLC

Physician| Neurologist | Irvine, CACity of Hope

Clinical Operations SpecialistA-Line Staffing Solutions LLC

Clinical Research CoordinatorUniversity of California, Irvine

Registered Nurse (RN) - Clinical Research Coordinator IIIntegrated Resources, Inc

Clinical Research AssistantCare Access

Clinical Research Coordinator, Full time, DaysPIH Health

Medical Assistant/Admit Worker - Center for Clinical Research - FT DaysUniversity of California, Irvine

Sr Research Associate IRD Partners

Market Research AssistantUltimate Staffing Services

Clinical Research Coordinator-RN IIIconma

Asst. Clinical Research Coordinator - HybridUniversity of California, Irvine

Associate Director, Clinical Science & External Research (Electrophysiology) - MedTechJohnson and Johnson

Clinical Research Coordinator-RN IIApidel Technologies

STEM Learning Lab Research AssistantUniversity of California, Irvine

Clinical Research Coordinator I (Huntington Beach, CA)Care Access

RN Clinical Research, Full time, 8am-4:30pmPIH Health

Clinical Research ManagerUniversity of California, Irvine

Clinical Research Manager - HybridUniversity of California, Irvine

ASST. RESEARCH DATA COORDINATOR - HYBRIDUniversity of California, Irvine

Research AssistantUniversity of California, Irvine

Clinical Research CoordinatorWake Research

Clinical Research NavigatorUniversity of California, Irvine

Research Assistant - Simply BiotechTalentZok

Temporary Clinical Research Coordinator (CRC)University of California, Irvine

Associate Tax Attorney (Research-focused)Jobot

Research Associate - II*Integrated Resources, Inc

Clinical Research CoordinatorFlourish Research

Research Data Coordinator - HybridUniversity of California, Irvine

Remote Market Research Assistant Earn Up to $50/TaskOccupons Quebec

(Remote) Data Entry Work From Home / Focus Research PanelistFocusGroupPanel

Research Associate IIITap Growth ai

Research Associate IITap Growth ai

Senior Tax Attorney of ResearchTalley LLP

Senior Research AssociateIconma

Research AssociateLancesoft

Senior Research Associate – Downstream Process Development (Protein Purification, AKTA, UF/DF, ADC)Pyramid, Inc

Vice President, Research Integrity & ComplianceUniversity of California, Irvine

Market Research InterviewerSensis

Specialized Tax Services - Research & Development Tax Senior ManagerPwC

Research Scientist - Simply BiotechTalentZok

Sr. Clinical Research RepresentativeOQSIE

Research Summer Intern ProteinZymo Research Corporation

Senior Associate, ResearchGreen Street Advisors, LLC

NASI - Lead Research & Development Engineer - Advanced Vehicle Development (AVD)Subaru of America, Inc.

Credit Research Analyst - Aristotle Pacific CapitalAristotle Capital Management

Part-Time/Full-Time Research Panel. Entry Level. Receptionist or Typist WelcomeApexFocusGroup

Audio Algorithm Architect, Applied ResearchGoogle

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