Clinical Research Coordinator II - California Heart Center Cedars-Sinai Medical CenterClinical Research Coordinator II - California Heart CenterBeverly Hills, CAPrimary Duties and Responsibilities: Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures, and labs, and completion and maintenance of consent forms, case report forms, SAE's, and source documents.
Clinical Research Assistant Providence Health & ServicesClinical Research AssistantSanta Monica, CA$25–$35.77 / hourRequsition ID: 446477 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Full time Job Shift: Day Career Track: Clinical Support Department: 7008 RHEUMATOLOGY CA SANTA MONICA Address: CA Santa Monica 2336 Santa Monica Blvd Work Location: SJHC Santa Monica 2336-Santa Monica Workplace Type: On-site Pay Range: $25.00 - $35.77 Our not-for-profit network provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care, and even our own Providence High School.
Assistant Clinical Research Coordinator - Pediatrics University of CaliforniaAssistant Clinical Research Coordinator - PediatricsLos Angeles, CA$30.74–$49.46 / hourHSR faculty conduct research with systems-level impact on child health in areas including childhood adversity, children with medical complexity, early childhood development, education and school systems, housing and health, obesity prevention, poverty, primary care and healthcare systems, vaccine delivery and uptake, and youth incarceration. The AMP ACEs project is a community-based research initiative designed to evaluate whether a telephone-based Adverse Childhood Experiences (ACEs) screening and care coordination model delivered through 211LA increases referrals to, and receipt of, ACEs-related services.
Clinical Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem) Cedars-Sinai Medical CenterClinical Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem)Los Angeles, CAThe job will provide an outstanding opportunity to work with a multidisciplinary team involving optical engineers, mechanical engineers, electrical engineers, biomedical engineers as well as surgeons, pathologists, and other medical personnel. The Butte Lab is developing novel intra-operative imaging/visualization technologies to aid surgeons in achieving near-complete tumor excision.
Clinical Research Associate I - CalHeart Cedars-Sinai Medical CenterClinical Research Associate I - CalHeartCAPrepare and submit documents to the IRB which includes initial site submission forms, continuing review reports, initial and revised consents, amendments to the protocol, investigator brochures, protocol deviations, SAE reports, and IND safety reports, close-out reports, patient provided documents, such as QOLs, letters, and diaries. CalHeart, affiliated with the Cedars‑Sinai Smidt Heart Institute, offers the full spectrum of cardiology care, including cardiac evaluation, heart failure management, interventional cardiology, nuclear cardiology, echocardiography and hypertension management.
Clinical Research Assistant Providence St. Joseph HealthClinical Research AssistantSanta Monica, CATogether, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. Supports the Clinical Research Department in managing the clinical trial patients by assisting with patient identification, screening, registration and clinical trial data collection.
Manager, Laboratory Services - Clinical Lab - Full Time 8 Hour Days (Exempt) (Non-Union) University of Southern CaliforniaManager, Laboratory Services - Clinical Lab - Full Time 8 Hour Days (Exempt) (Non-Union)Los Angeles, CA$151,424–$249,850 / yearWhen 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. As Manager, the individual is responsible for technical and staff supervision, administrative management of all sections and for assuring proficiency of staff, accurate instrument operation, performance of maintenance and troubleshooting measures, quality control, quality assurance and proficiency testing.
Clinical Relations Manager - West Coast Glaukos CorpClinical Relations Manager - West CoastLos Angeles, CAOur constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Lead Clinical Research Analyst - Hematology/Oncology (Santa Monica) University of CaliforniaLead Clinical Research Analyst - Hematology/Oncology (Santa Monica)Santa Monica, CA$100,170–$218,715 / yearThe 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. The Clinical Research Analyst 4 plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout.
Assistant Clinical Research Coordinator - Hematology/Oncology University of CaliforniaAssistant Clinical Research Coordinator - Hematology/OncologyLos Angeles, CA$27.08–$43.55 / hourThe 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.
Senior Clinical Research Coordinator - Hematology/Oncology (Santa Monica) University of CaliforniaSenior Clinical Research Coordinator - Hematology/Oncology (Santa Monica)Santa Monica, CA$82,705.68–$133,068.24 / yearThe 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.
Clinical Research Coordinator II - Medical Group Cedars-Sinai Medical CenterClinical Research Coordinator II - Medical GroupBeverly Hills, CAPrimary Duties and Responsibilities: Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all applicable regulatory requirements.
Director, Clinical Affairs Saluda Medical Pty LtdDirector, Clinical AffairsCAWhat Youll Do: Development, maintenance, and optimization of the clinical quality system, clinical regulatory requirements, and data integrity/quality Establish detailed program plans, drive program execution toward established objectives, assess risk and implement strategies to ensure successful delivery of the clinical objectives Contribute to the overall strategic direction for development and implementation of clinical affairs objectives and processes Direct and collaborate with internal and external staff to assure successful conduct of assigned clinical programs consistent with company objectives and applicable regulations and policies Development of protocols, statistical analysis plans, reports and other clinical study documentation Support and contribute to manuscripts, abstracts, data presentations, and health economic value initiatives Promote and embody culture and behavior expectations of a high-performance culture Drives leadership of issue identification and resolution. Knowledge/Skills/Abilities: Excellent verbal and written communication Ability to think creatively, dynamically, and foster a culture of commitment to thoughtful science to help patients in need Knowledge of ICH/GCP and FDA medical device regulations Knowledge of electronic data capture systems and web-based clinical trial management tools Knowledge of research design, data analysis and biostatistics Self-motivated and independent work style with the ability to initiate and follow through on assignments Self-assured, knowledgeable professional capable of developing good interpersonal relationships with medical professionals Excellent organizational skills and attention to detail High degree of personal integrity.
Clinical Research Coordinator III (Hybrid) Cedars-Sinai Medical CenterClinical Research Coordinator III (Hybrid)Beverly Hills, CAThe Clinical Research Coordinator III 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. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Clinical Research Coordinator I -Surgery Chair Cedars-Sinai Medical CenterClinical Research Coordinator I -Surgery ChairLos Angeles, CAThe Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Contractor- Assistant Clinical Research Coordinator (Pasadena, CA) Profound Research LLCContractor- Assistant Clinical Research Coordinator (Pasadena, CA)Pasadena, 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.
Clinical Research Associate 1 Allen SpoldenClinical Research Associate 1Los Angeles, CaliforniaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Senior Clinical Research Associate IRESenior Clinical Research AssociateLos Angeles, California$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. Senior Clinical Research Associate- Oncology- Los Angeles, CA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate II IREClinical Research Associate IILos Angeles, California$91,336–$114,170 / yearWilling 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. Clinical Research Associate- Oncology- West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
NewLicensed Program Assistant Loudoun CountyLicensed Program AssistantSterling, VA$44,419.88–$73,292.81 / yearResponsibilities include, but are not limited to: Provides administrative support to our licensed programs, including both preschool and childcare programs, with administrative support for special projects and various functions and meetings. Employees hired into Regular Part-Time Intermittent positions are eligible for limited County employee benefit programs, based on the position's regularly scheduled hours.