Staff Research Associate 2 - OBGYN UCLA Health SystemStaff Research Associate 2 - OBGYNLos Angeles, CA$32.79–$52.75 / hourUnder the mentorship of Dr. Memarzadeh, you will work as a full-time Staff Research Associate II and will perform a variety of molecular, cellular and genomic research techniques (flow cytometry, IHC, proteomics, transcriptomics) while working on projects related to understanding the immunologic and genetic events involved in the formation and progression of gynecologic disease. The Gynecologic Oncology (GO) Discovery lab (godiscoverylab.com) investigates the molecular pathways in chemotherapy-resistant ovarian and aggressive endometrial tumor cells that are candidates for therapeutic intervention via small molecule inhibitors and/or immunotherapy.
Staff Research Associate 3 UCLA Health SystemStaff Research Associate 3Los Angeles, CA$75,439.44–$121,333.68 / yearWorking closely with faculty, researchers, trainees, and external collaborators, the SRA III will contribute to the development of innovative assays, generation of high-quality research data, and advancement of scientific publications and grant-funded projects. The successful candidate will manage and maintain state-of-the-art instrumentation, perform quality control and data analysis, and oversee essential laboratory operations such as inventory management, reagent procurement, regulatory compliance, and equipment maintenance.
Research Associate Terasaki Institute for Biomedical InnovationResearch AssociateWoodland Hills, CAPerforms laboratory experiments including histology, molecular biology, imaging, cell and animal modeling, and sequencing under supervision and guidance by a senior researcher following appropriate training to support innovative science, including translational applications of neuromodulation technologies to metabolic and inflammatory diseases. Bachelor of Science (or similar) in Medical Technology, Biology or Chemistry, Biotechnology, Diploma in Laboratory Science or Medical Laboratory Technology, or recent molecular biology laboratory experience.
Nurse Practitioner- Research -Per Diem UCLA Health SystemNurse Practitioner- Research -Per DiemLos Angeles, CABy using the SPs the NP is able to change treatment regimen after observing signs and symptoms of illness, reactions to treatment, general behavior and physical condition, and determines if they are abnormal findings (Ca Nursing Practice Act, subsection(b) of Section 2725). In the Research NP role, the NP will promote the ethical care of research patients and liaison with principle investigators to care for clinical trial patients, as well as provide education and support, make appropriate referrals and document services rendered.
Research Pharmacist / Intermittent Parexel International CorpResearch Pharmacist / IntermittentGlendale, CAActual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location. In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives.
Clinical Research Coordinator ATD Technology LLCClinical Research CoordinatorFullerton, CA$45Oncology Clinical Research Coordinator General Summary: Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Minimum 2 years' experience in a clinical research setting where candidate managed patients (consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data).
Research Coordinator - Neurology UCLA Health SystemResearch Coordinator - NeurologyLos Angeles, CA$27.08–$43.55 / hourb'nn n n n n n n n n n n n nn n n n n n n n n n n n n n n n n n Research Coordinator - Neurology - - 30659 - UCLA Healthn n nnnn nn n n n nn n n n n Skip to content nn n n n n n UCLA Health Home Page n n nn nnn n nn n Main menu. Press enter or space keys to expands and escape key to collapse nn n n n n n n Search jobs n n nn ...
Senior Clinical Trials Manager ImmunityBio IncSenior Clinical Trials ManagerEl Segundo, CAImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response.
Senior Clinical Site Budget Specialist ImmunityBio IncSenior Clinical Site Budget SpecialistEl Segundo, CAGuide and support clinical operations departments in the site budgeting process for ImmunityBio trials, as well as investigator initiated trialsincluding the preparation, negotiation and execution of clinical trial budgets, service contracts and agreements. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response.
NewResearch & Development Manager O PositivResearch & Development ManagerSanta Monica, California$135,000–$160,000 / yearOur growing portfolio spans PMS & hormone balance, vaginal & urinary health, digestion, menopause, and conception support—offering vitamins, supplements, and personal care products that women trust. Since launching in 2018, O Positiv has reshaped the women’s health space, tackling long-overlooked issues with innovative, science-backed products and boldly breaking taboos along the way.
Research Scientist, Biomarker Sciences I* The Fountain Group LLCResearch Scientist, Biomarker Sciences I*Santa Monica, CA$40–$47.36 / hourThis role will work at the intersection of Research and Clinical Development, supporting pharmacology, biomarker strategy, clinical trial execution, translational analyses, and regulatory submissions. Collaborate with Clinical Operations, Regulatory, Clinical Data Management, Biometrics/Statistics, Bioinformatics, and Translational Medicine teams.
Research Administrator UCLA Health SystemResearch AdministratorLos Angeles, CA$35.23–$53.67 / hourAs 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. Perform post-award and other financial management and analysis for the Clinical AIDS Research and Education (CARE) Center in the Department of Medicine at UCLA.
Associate Director, Clinical Costing Systems & Tools BeOne Medicines AGAssociate Director, Clinical Costing Systems & ToolsCA$141,600–$191,600 / yearThis role, sitting at the intersection of clinical trial operations and technical engineering, will be responsible for supporting the technical design of robust resourcing and costing methodologies, work with functional teams to develop and review costing algorithms, and ensure seamless integration of our tools with internal systems across clinical trial functions (CTMS, EDC etc.), Resource Management, Finance (SAP etc.), HR (Workday etc), and IT in support of accurate study level internal & external cost estimation as well as forecast of resource requirements. The ideal candidate brings sound technical, engineering, operational and system development knowledge & experience within CRO or biopharmaceutical industry, ability to translate complex operational, resource estimation and pricing requirements into technical roadmaps, strong analytical and systems-thinking capabilities, and exceptional cross-functional communication skills.
Clinical Research Coordinator II Actalent IncClinical Research Coordinator IIGlendale, CA$33–$40 / hourThis role focuses on screening, recruiting, and consenting patients, performing study-related patient visits and procedures, and collaborating closely with data and regulatory teams to ensure accurate documentation and compliance with study protocols. The Clinical Research Coordinator works within a collaborative oncology research team that includes full-time and part-time coordinators, research assistants, data management staff, regulatory staff, and project management support.
Clinical Research Coordinator III Actalent IncClinical Research Coordinator IIILos Angeles, CA$33–$40 / hourThis role focuses on screening, recruiting, and consenting patients, performing study-related patient visits and procedures, and collaborating closely with data and regulatory teams to ensure accurate documentation and compliance with study protocols. The Clinical Research Coordinator works within a collaborative oncology research team that includes full-time and part-time coordinators, research assistants, data management staff, regulatory staff, and project management support.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorFountain Valley, CA$28–$35 / hourConduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring. 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.
Travel Clinical Research Coordinator - California ECN Operating LLCTravel Clinical Research Coordinator - CaliforniaLos Angeles, CA$70,000–$75,000 / yearThe Travel Clinical Research Coordinator collaborates with investigators, sponsors, CROs, and site staff while maintaining compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines. The Travel Clinical Research Coordinator plays a key role in supporting new research sites through study opening activities and early enrollment efforts for our sites in California.
Clinical Research Program Manager - Women's & Guerin Children's - Full-Time, On-Site Cedars-Sinai Medical CenterClinical Research Program Manager - Women's & Guerin Children's - Full-Time, On-SiteLos Angeles, CACollaborate with internal and external key stakeholders including other departments, leaders across the organization, representatives from external agencies/organizations in the management of the program to provide guidance, resolve issues, grow the program, and/or implement processes and/or solutions. You will be responsible for directing and managing specified programs and will provide leadership, guidance and direction for the day-to-day clinical research operations and activities, including authority to make independent decisions regarding program operations, administration, and governance.
Clinical Research Budgeting Analyst - Remote Providence Health & ServicesClinical Research Budgeting Analyst - RemoteCalifornia, CARemote$37.84–$58.75 / hourIt is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Main responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budget milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments.
Research Nurse IV, LPN/LVN, Clinical Trials Kaiser PermanenteResearch Nurse IV, LPN/LVN, Clinical TrialsLos Angeles, CAConducts and leads clinical research by: reviewing, designing, and collecting clinical trials data; leveraging an advanced knowledge of source data and the tools leveraged for analyzing, and interpreting clinical data; leveraging advanced knowledge when providing input on the design of clinical trials, studies, and interventions at the site-level; developing innovative clinical research protocols and other processes of large-scale clinical trials; preparing, submitting, and/or collaborating with others to ensure correct compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for executing clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in various research lab operations (e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens). Ensures documentation of clinical research files by: ensuring the timely, accurate, and complete documentation of all research activities (e.g., consent forms, reports, tracking forms); contributing to the development and/or implementation of moderately complex quality control and/or assurance measures and providing feedback to research staff and management; assessing volunteers and/or patients for eligibility to participate in Clinical Trials, escalating when necessary; and monitoring and auditing Clinical Trials across sites and presenting findings to KP leadership.