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Oncology Clinical Research Coordinator Jobs in Los Angeles, California

Dps Clinical Research Coordinator
By City of Hope At Duarte, CA, United States
Bachelor’s Degree or Certified CRA or Certified Tumor Registrar in lieu of degree. Experience may substitute for minimum education requirements.
Basic education, experience and skills required for consideration:
Preferred education, experience and skills:
Conducts protocol database management for an assigned set of multiple research protocols.
Makes recommendations and participates in Policy and Procedure development regarding particular areas of team assignment and general data management issues.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.
Clinical Research Coordinator Jobs
By Care Access At Los Gatos, CA, United States
Good management and organizational skills, understanding of medical procedures
Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelines
Exceptional interpersonal skills, the ability to work independently
Phlebotomy experience is a plus
Experience checking and documenting vitals and EKG (ECG) within the past year.
Benefits (US Full-Time Employees Only)
Clinical Research Coordinator - Obgyn
By UCLA Health At , Los Angeles, 90095, Ca $24.28 - $48.04 an hour

Description To support Clinical Trials, The Department of OBGYN is seeking to hire a full time Clinical Research Coordinator. You will work with the PI, Sub-Investigators, research personnel and ...

Clinical Research Coordinator Jobs
By Shriners Children's At Pasadena, CA, United States

Shriners Children’s is a family that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global ...

Clinical Research Coordinator Jobs
By SMCI At San Francisco Bay Area, United States
Education: BS/BA degree in a life science, health science, RN, or related field.
2+ years of professional working experience as a Clinical Research Coordinator.
Working knowledge of GCP and FDA Regulations.
Excellent oral and written communication skills.
Strong attention to detail and organizational skills.
Experience utilizing Electronic Data Capture (EDC) systems for clinical studies.
Clinical Research Coordinator Jobs
By Rady Children's Hospital-San Diego At San Diego County, CA, United States

Job Summary: Initiates & manages multiple cooperative group trials such as Children's Oncology Group (COG) clinical trials related to pediatric cancer to include, but not limited to: execution ...

Ptsd Assistant Clinical Research Coordinator
By UC San Diego Health At , San Diego, 92093, Ca $31.04 - $49.94 an hour
Experience in neuropsychological assessment and patient interviewing to determine participant impairment as defined by protocol management.
Experience using statistical software applications. Knowledge of database, word processing and spreadsheet applications such as Velos, Access, Excel and MS Word.
Experience performing clinical research duties in a clinical research environment.
Experience with clinical trials participant or study subject recruitment.
Experience coordinating study startup activities.
Experience providing in-service training to various research personnel on protocols, processes, and procedures.
Clinical Research Assistant - Oncology
By Scripps Health At La Jolla, CA, United States
Focus on data entry, patient follow up visits and phone calls.
Coordinate multiple aspects of clinical trials and other human research ensuring compliance with research protocol and IRB requirements.
Manage regulatory documents and data submission, assists with IRB submissions, responsible for keeping internal data tracking systems up-to-date.
Provide superior service to principal investigators and research sponsors within scope of responsibilities.
Advanced written, oral and interpersonal communication skills.
Strong prioritization, organizational, and problem solving skills.
Clinical Research Coordinator Jobs
By care.coach At Millbrae, CA, United States
Strong attention to detail & time management skills
Implement and manage clinical research projects with internal and external stakeholders across the country in hospital and community-based settings
Obtain IRB approval and maintain compliance with OHRP and other federal regulatory requirements
3+ years of research coordination experience and independence (can be pre-doctoral)
Experience with older adults and ab/normal age-related decline
Grant writing and clinical trial (RCT) experience
Clinical Research Coordinator Jobs
By Insight Global At Spring Valley, CA, United States
Desired Skills and Experience *
Data Entry, Administrative needs - i.e. Filing, set-up for upcoming appts, organizing documentation, and Patient consenting
PART TIME- 20 Hours Per Week
Contract Duration: 6 Months with potential to extend!
Senior Scientist I, Translational Immuno-Oncology Research, Precision Medicine Oncology
By AbbVie At South San Francisco, CA, United States
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
Proficiency in immune cell-based assays, molecular techniques, and strong technical skills in performing multiparameter flow cytometry and data analysis.
Ph.D with postdoctoral research experience in cancer therapeutics targeting immune cells and epigenetics or related field in academia or pharma industry.
Experience working with CRO in designing and executing projects and experiments is highly desired
Hands-on experience in generating and analyzing multi-parameter gene and protein datasets is highly desirable (RNASeq, Nanostring, scRNASeq, etc.)
Ability to work independently and proactively on multiple projects in a fast-paced environment.
Clinical Research Coordinator Jobs
By City of Hope At Irvine, CA, United States
Bachelor’s Degree. Experience may substitute for minimum education requirements (Associate Degree plus minimum of 2 years of experience).
Two or more years of experience related to the management and conduct of oncology clinical trials in an academic setting.
Basic education, experience and skills required for consideration:
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.
Clinical Research Coordinator Jobs
By ProSciento, Inc. At Chula Vista, CA, United States
Keeps the Clinical Trial Management System (CTMS) updated with pertinent information.
Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.
Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities.
Assists with data entry, as needed.
Communicates with study subjects regarding their study status and enrolment into the study.
Schedules subject appointments, performs subject reminder calls, and instructs subjects regarding any medication washout per protocol.
Clinical Research Coordinator Jobs
By Truvian At San Diego, CA, United States
Maintain working knowledge of multiple Institutional Review Boards (IRB) approved protocols and assist with data entry as needed
Clinical Site Management, including implementation of associated processes and documentations
Manage sign up calendar for available appointments for upcoming studies
Manage phlebotomist scheduling with external vendor
Record adverse events for donors experience in draw session
Maintain good record keeping of compensation log per donor and collaborate with Finance team to address pay out concerns
Clinical Research Consortia Coordinator-Remote
By UC San Diego Health At , San Diego, 92103, Ca $29.99 - $48.25 an hour
Experience with data management tools such as REDCap.
Experience using statistical software applications. Knowledge of database, word processing and spreadsheet applications such as Velos, Access, Excel and MS Word.
Experience interpreting medical charts, experience in abstracting data from medical records.
Experience with clinical trials participant or study subject recruitment.
Experience coordinating study startup activities.
Experience providing in-service training to various research personnel on protocols, processes, and procedures.
Clinical Scientist, Oncology Early Development
By ABBVIE At , San Francisco, Ca
Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols
We offer a comprehensive package of benefits including paid time off. (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees
Collaborate cross-functionally to help create a scientific platform in support of the regulatory, commercial and medical education strategy for late-stage assets.
Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.
Responsible for providing focused scientific and clinical study support from start-up clinical study report (CSR).
Contribute to creation of electronic database, IRT, and associated training documents and review data completeness and fidelity throughout study conduct.
Clinical Research Coordinator Jobs
By Carbon Health At San Francisco, CA, United States
Minimum of 1-year related experience with clinical research
Knowledge of research ethics and regulations
Excellent communications skills (verbal and written) and interpersonal skills are required
Comprehensive benefits package including medical, dental & vision insurance
All benefits dependent on role and eligibility
120+ locations and growing, along with vast virtual coverage
Clinical Research Coordinator - Hybrid/Remote - 122856
By UC San Diego Health At San Diego, CA, United States
Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
Strong knowledge of investigational protocols especially with pediatric protocols (data management, query resolution, protocol design, protocol writing and protocol implementation).
Demonstrated experience in clinical trials research. Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
Demonstrated experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Clinical Trial Research Nurse I, So. San Francisco, Oncology -Experience Preferred!
By Kaiser Permanente At , San Francisco, Ca $148,200 - $191,730 a year
W/ supervision, assist in the accurate & appropriate study test article management.
Support the effective financial management of the clinical trial.
Must be able to work in a Labor/Management Partnership environment.
Assist in the identification & procurement of equipment & supplies needed to fulfill protocol requirements.
High School Diploma or General Education Development (GED) required.
Demonstrate effective written, verbal, and interpersonal communication skills.
Research Scientist Ii, Immuno-Oncology - Car-T
By Poseida Therapeutics Inc At , San Diego, 92121, Ca $100,000 - $125,000 a year
Requirements, Knowledge, Skills and Abilities
Hands-on experience in developing and characterizing CAR-T cell products is highly preferred
Experience in developing in vivo models and executing in vivo studies
Experience analyzing and interpreting large, complex data sets - experience with ‘omics’ methods for cell characterization is a plus.
Excellent oral and written communication skills with proven ability to work well independently and as part of a team
Drive efforts to develop next-generation CAR-T cell therapies