NewClinical Research Coordinator JouléClinical Research CoordinatorSan Diego, CA$26–$30 / hourProficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
NewCorporate Associate (Licensing) JobotCorporate Associate (Licensing)San Diego, CA$230,000–$350,000 / yearInformation 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. Our client, a highly regarded law firm with a nationally recognized Life Sciences and Technology Transactions practice, is seeking a Licensing Associate with at least 3 years of relevant experience to join its growing team.
Senior Clinical Research Associate Crinetics Pharmaceuticals IncSenior Clinical Research AssociateCA$119,000–$149,000 / yearTrain and assist site coordinators, investigators, and CRO (as applicable) in collecting data and executing the study in a timely manner that meets the protocol requirements and timelines/milestones; serve as a resource to site coordinators, investigators and other staff members regarding investigational products and protocols. Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate visit reports and letters in a timely manner.
Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available Thermo Fisher ScientificExperienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas AvailableSan Diego, CaliforniaAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateSan Diego, CA$110,520–$138,150 / yearPerform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Clinical Research Associate, Sponsor Dedicated, IQVIA IQVIA Holdings IncClinical Research Associate, Sponsor Dedicated, IQVIACarlsbad, CA$71,900–$182,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)San Diego, CaliforniaFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Associate - Sponsor Dedicated IQVIA Holdings IncClinical Research Associate - Sponsor DedicatedCarlsbad, CA$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Senior Clinical Research Associate, Sponsor Dedicated IQVIASenior Clinical Research Associate, Sponsor DedicatedCarlsbad, CaliforniaEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Associate, Sponsor Dedicated IQVIAClinical Research Associate, Sponsor DedicatedCarlsbad, CaliforniaPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Clinical Research Associate II/ Oncology & Ophthalmology/ West region of the US! Thermo Fisher Scientific IncClinical Research Associate II/ Oncology & Ophthalmology/ West region of the US!San Diego, CA$80,000–$125,000 / yearWhat You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
NewClinical Research Associate Actalent IncClinical Research AssociateSan Diego, CA$38–$65 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources Rady Children's HospitalClinical Research Coordinator (Non-RN) - Hematology/Oncology Research ResourcesSan Diego, CA$34.14–$46.94 / hourResponsibilities may include but are not limited to: submission of protocols & renewals to IRB & scientific review boards; management & submission of electronic data forms to Sponsors, CROs & regulatory agencies; screening for eligibility; monitoring and timely reporting of adverse events; toxicities and protocol deviations; scheduling subjects' visits; coordinating clinical, laboratory and data management activities; processing and submitting laboratory specimens. Assist with initiation, implementation and management of research projects in accordance with GCP, FDA, HIPAA & all required regulatory guidelines, with an emphasis on pediatric clinical research studies.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedCarlsbad, CA$71,900–$189,000 / yearPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Senior Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncSenior Clinical Research Associate, Sponsor DedicatedCarlsbad, CA$74,500–$197,500 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Associate University of Southern CaliforniaClinical Research AssociateSan Diego, CA$36.36–$50.90 / hourThe USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
Sr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIACarlsbad, CADeprecated : preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85 .
Clinical Research Coordinator Odyssey Systems Consulting Group, Ltd.Clinical Research CoordinatorSan Diego, CaliforniaFull timePosition Summary: Odyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated with conducting Traumatic Brain Injury Center of Excellence (TBICoE) clinical investigations in TBI, brain health, and related outcomes. Prepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentations and requirements as Facilitates the flow and approval processes for relevant projects as needed or requested.
Clinical Research Coordinator Medical Oncology Associates of San DiegoClinical Research CoordinatorSan Diego, CaliforniaThe Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Additional duties and responsibilities: Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
Clinical Research Coordinator (RN) - Research & Clinical Management - Genomics Rady Children's HospitalClinical Research Coordinator (RN) - Research & Clinical Management - GenomicsSan Diego, CA$71.31–$99.17 / hourThe CRC's primary responsibilities are related to study management which includes supervising and educating the study team, subject recruitment and protocol implementation strategies, preparing study source documents, flowcharts and checklists, monitoring study team compliance and executing the research protocol clinical procedures. Functions as a role model at the expert level of clinical and research practice, characterized by viewing situations as a whole, advanced clinical skills, teaching/mentoring of peers and direct reports and professional contributions to research.
Clinical Research Coordinator (San Diego, CA)* Profound Research LLCClinical Research Coordinator (San Diego, CA)*Carlsbad, CAYou'll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. Bachelor's degree with 1+ year of relevant experience, OR Associate's degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience.
Contractor- Assistant Clinical Research Coordinator (Oceanside, CA) Profound Research LLCContractor- Assistant Clinical Research Coordinator (Oceanside, CA)Oceanside, CAAs an Assistant Clinical Research Coordinator at Profound Research, you'll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate's degree with 1+ year of relevant experience, OR Bachelor's degree with relevant coursework or experience in a clinical or life sciences setting.
Sr Clinical Research Coord Non-RN - Hematology Oncology Research Resources Rady Children's HospitalSr Clinical Research Coord Non-RN - Hematology Oncology Research ResourcesSan Diego, CA$37.63–$51.75 / hourIn addition to having mastered the competencies of the intermediate CRC, the senior CRC demonstrates advanced skills and knowledge along with the ability to support, guide, train, demonstrate or lead study team members in the implementation or study related activities. The senior CRC contributes to the development of new processes, procedures, tools, and training to enhance clinical research activities across the competency domains and conducts quality assurance / quality control checks of the work of others.
Contractor- Clinical Research Coordinator (Oceanside, CA) Profound Research LLCContractor- Clinical Research Coordinator (Oceanside, CA)Oceanside, CADiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that's rare in a single organization (for Clinical / Patient-Facing roles). You'll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams.
Clinical Research Coordinator I CAMRISClinical Research Coordinator ISan Diego, CAFull timeIn addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted. Manage and coordinate complex clinical trials: Handle complex logistics of trials, solve problems related to compliance or participant concerns, and make adjustments to protocols based on emerging situations during the study.
Senior Clinical Research Coordinator Headlands Research IncSenior Clinical Research CoordinatorSan Diego, CA$70,304–$75,000 / yearManaging all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines.
Clinical Research Coordinator ECN Operating LLCClinical Research CoordinatorSan Diego, CA$20–$24 / hourThe CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred , as this role may include specimen collection and basic clinical procedures.
Senior Clinical Research Coordinator (51328) West DermatologySenior Clinical Research Coordinator (51328)San Diego, CAResponsibilities: Perform all research coordinator duties required to adhere to FDA guidelines and study protocols, and facilitate the daily clinical trial activities required to conduct the study, including, but not limited to: Subject recruitment, screening, and enrollment. Company Conformance Statements: In the performance of their respective tasks and duties, all employees are expected to conform to the following: Perform quality work within deadlines with or without direct supervision.
Bilingual Part-Time Clinical Research Coordinator Actalent IncBilingual Part-Time Clinical Research CoordinatorEncinitas, CA$25–$33 / hourEngage in community outreach by visiting clinics/hospitals, distributing recruitment materials, educating medical staff, and maintaining online recruitment portals. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Senior Clinical Trial Associate Crinetics Pharmaceuticals IncSenior Clinical Trial AssociateCA$83,000–$104,000 / yearContribute to study start-up, conduct, and closeout activities including, but not limited to, create patient facing materials, draft newsletters and site memos, track study metrics and escalate issues to study team Perform project/study management-related responsibilities from inception through database lock by coordinating and tracking activities for protocol and SOP compliance as well as regulatory guidelines. Typically working on assignments requiring judgement and initiatives with an understanding of the implications of the work being performed, the Senior CTA independently identifies tasks/issues that need to be addressed while being highly organized with the ability to multitask and adjust direction based on changing project/corporate priorities.
Clinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations Nationwide Headlands ResearchClinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations NationwideSan Diego, CA$45,000–$100,000 / yearThis general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.
Principal Research Associate/ Toxicology Study Coordinator Ionis Pharmaceuticals IncPrincipal Research Associate/ Toxicology Study CoordinatorCarlsbad, CA$110,847–$142,160 / yearWith multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals. This position reports to the Vice President of Toxicology and works closely with toxicologists and the Toxicology Operations team to coordinate study activities, support data review, and address departmental operational priorities.
Senior Clinical Research Coordinator Salma HealthSenior Clinical Research CoordinatorLa Jolla, California$72,000–$90,000 / yearWe are the brain health company of the future, integrating care delivery, technology innovation, and research breakthroughs to better understand brain biology and diagnose, treat, and ultimately cure brain disorders across all stages of life. This role actively drives and manages relationships with study sponsors and CROs, and serves as the site’s primary point of contact for sponsors, IRB submissions, and research participants.
Senior Clinical Research Coordinator Headlands ResearchSenior Clinical Research CoordinatorSan Diego, CaliforniaManaging all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines.
Senior Director, Clinical Pharmacology & Pharmacometrics, Research Business Insights & Technology Bristol Myers SquibbSenior Director, Clinical Pharmacology & Pharmacometrics, Research Business Insights & TechnologySan Diego, CA$252,640–$306,137 / yearThis leader will partner deeply with Clinical Pharmacology, Pharmacometrics, Quantitative Pharmacology, and Translational Medicine stakeholders to deliver the applications, modeling environments, workflow automation, and governed operational capabilities that support CPP work end to end-from quantitative preclinical-to-clinical bridging through clinical PK/PD, dose and regimen decisions, and submission-support outputs. The role carries accountability for the reliability, fit-for-purpose evolution, and long-term scaling of the CPP technology stack and workflow ecosystem, while working in a highly matrixed model with scientific leaders, data teams, lab-platform teams, and regulatory-facing partners.
Research Associate - Associate-Senior RD PartnersResearch Associate - Associate-SeniorSan Diego, California£114,999–£143,748Collaborate with research, analytical development and process development teams to develop, qualify/validate AAV gene therapy analytical/molecular biology assays, chemical/biochemical assays, and cell-based biological potency assays, for process monitoring and product release and stability, e.g., compendial methods, HPLC, DLS, droplet digital PCR or qPCR, ELISA, and cell based potency assays. · Experience in pharmaceutical industry with a GMP testing focus, ideally covering the analytical method and testing lifecycle from development through commercial drug product testing, with experience in a GMP QC release testing role.
Principal Research Associate/ Toxicology Study Coordinator Ionis Pharmaceuticals Inc.Principal Research Associate/ Toxicology Study CoordinatorCarlsbad, CA$110,847–$142,160 / yearWith multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals. This position reports to the Vice President of Toxicology and works closely with toxicologists and the Toxicology Operations team to coordinate study activities, support data review, and address departmental operational priorities.
NewResearch Associate - III Integrated Resources, IncResearch Associate - IIISan Diego, CaliforniaContractorThe candidate should be able to apply different research techniques in the work including immune cell purification, ELISA and luminex assays, FACS, RNA extraction and RTPCR.Experience with animal work and lymphoid organ collection would be ideal. Job DescriptionThe candidate should have a MS/PhD in biological science with research experience in cellular and molecular immunology and hands-on work experience in cell-based assays using purified immune cells from human or mouse.
Clinical Research Manager Headlands Research IncClinical Research ManagerEscondido, CA$100,000–$105,000 / yearLead regular team meetings to discuss status of current projects, plan for future projects, provide updates on new company initiatives, seek feedback regarding team barriers, etc. Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
NewResearch Associate III Integrated Resources, IncResearch Associate IIISan Diego, CaliforniaContractorJob DescriptionThe person will be responsible for developing cell based assays for compounding screening and will analyse the cell responsesQualifications• The candidate should have a minimum of BS/MS in biological sciences with substantial training in molecular pharmacology, biochemistry and/or immunology.• Hands-on experience (3-5 years) with diverse cell-based assays for compound screening is essential, particularly analysis of cell responses using ELISA, MSD, Luminex, FACS and imaging readouts.•
NewResearch Associate II Integrated Resources, IncResearch Associate IISan Diego, CaliforniaContractorThe individual will be actively involved in laboratory work related to the dosing and sampling of molecules, raw materials, and-or blood and tissues for the determination of pharmacokinetic properties of new therapeutics coming from various research targets through in vivo experimentation.• Research Associate IIA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Research Associate Odyssey Systems Consulting Group, Ltd.Research AssociateSan Diego, CaliforniaFull timeIn this role, you will participate in aspects of research including but not limited to recruiting and consenting participants in the clinic or in operational field settings, data collection and organization, literature reviews, structured interviews, analysis and interpretation of basic data, and preparation of data files, technical reports, summaries and protocols. Please Note: Final compensation for this position will be determined by various factors such as the Federal Government contract labor categories and contract wage rates, relevant work experience, specific skills and competencies, geographic location, education, and certifications.
Preclinical Veterinary Research Associate I, II, or III Pharmaron Beijing Co LtdPreclinical Veterinary Research Associate I, II, or IIISan Diego, CA$25–$35 / hourPharmaron San Diego is seeking a motivated Preclinical Veterinary Research Associate I, II, or III to join our Ophthalmology team supporting preclinical translational research programs focused on innovative ophthalmic therapeutics. This is an excellent opportunity for candidates with preclinical research, veterinary research, or in vivo laboratory experience who are looking to expand their technical skills and grow within a fast-paced and scientifically driven organization.
Advanced Research Associate - Chemistry Bio-TechneAdvanced Research Associate - ChemistrySan Marcos, California$52,000–$85,600 / yearDevelop and manufacture OEM diagnostic controls and calibrators for clinical chemistry and immunoassay applications including Cardiac Markers, Immunochemistry, Lipids, Urinalysis, Coagulation, Tumor Markers, and other protein orsmall moleculeanalytes. Minimum Job Requirements: Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred with 1-5 years work experience in In Vitro diagnostics, medical device, pharmaceutical or related industry required.
Clinical Research Coordinator Assistant - Psych University of CaliforniaClinical Research Coordinator Assistant - PsychSan Diego, CARemoteCareers at UC San Diego CHECK MY STATUS Search All Jobs Toggle navigation Overview Our Culture You Belong Here Veterans Living in San Diego Our Benefits Employee Career Development Jobs by Category UCSD Staff UCSD Health and Health Sciences Staff Internal Opportunites Academic/Faculty New Graduates Temporary Employment Professional Specialties Finance Information Technology Laboratory Professionals Nursing Staff Research Remote Opportunities Job Seeker Resources Check My Status Application Tips Help FAQs Getting Help Overview Our Culture You Belong Here Veterans Living in San Diego Our Benefits Employee Career Development Jobs by Category UCSD Staff UCSD Health and Health Sciences Staff Internal Opportunites Academic/Faculty New Graduates Temporary Employment Professional Specialties Finance Information Technology Laboratory Professionals Nursing Staff Research Remote Opportunities Job Seeker Resources Check My Status Application Tips Help FAQs Getting Help A CAREER THAT TRANSFORMS Whatever your role at UC San Diego, you help create a better world. General Data Protection Regulation (GDPR) Statement for Persons in the European Economic Area Privacy HIPAA Agreements Contact Us Maps & Tours Diversity Matters Disability Resources Employment Notices Principles of Community Volunteer at UC San Diego Health Volunteer at UC San Diego Getting to Campus Getting to Health System Divisions and Schools + Arts and Humanities Biological Sciences Graduate Division Jacobs School of Engineering Physical Sciences Rady School of Management School of Global Policy & Strategy School of Medicine Scripps Institution of Oceanography Skaggs School of Pharmacy * Social Sciences Regents of the University of California.
Assistant Clinical Research Coordinator - Psych University of CaliforniaAssistant Clinical Research Coordinator - PsychSan Diego, CARemoteUC San Diego is a student-centered, research-focused, service-oriented public institution recognized as one of the top fifteen research universities worldwide, and a top ten public university. 15 years later, my work improves operational efficiencies, provides valuable programs to the university, and even helps students bring their innovations to life.
Research Associate I, II, III - Large Animal Pharmaron Beijing Co LtdResearch Associate I, II, III - Large AnimalCarlsbad, CA$25–$35 / hourFounded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. The successful candidate will work alongside experienced scientists, veterinarians, and study teams in a fast-paced CRO environment, contributing directly to translational research programs that help advance new technologies toward clinical development.
Sr Research Associate I RD PartnersSr Research Associate IOceanside, California£81,402–£101,755Develop 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.
Research Associate - Chemistry Bio-Techne CorpResearch Associate - ChemistrySan Marcos, CA$42,400–$69,500 / yearMinimum Job Requirements: Bachelor's degree in Chemistry, Biochemistry, Biological Science, or related field preferred with 1-3 years work experience in In Vitro diagnostics, medical device, pharmaceutical or related industry required. By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics.
Research Data Associate Odyssey Systems Consulting Group, Ltd.Research Data AssociateSan Diego, CaliforniaFull timeThe role requires proving assurance of accurate documentation in compliance with all governing regulations for the collection, validation, and analysis of TBI- relevant research and outcomes data, and incudes interaction with relevant TBI stakeholders and to elicit and document business needs when modifying existing or creating new system functionality. Position Summary: Odyssey is looking for a Research Data Associate to design, develop and implement web-based applications to support data management activities associated with clinical investigations to support the Traumatic Brain Injury Center of Excellence (TBI CoE).