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Research Clinical Coordinator Jobs in San Diego, California

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 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!
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 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.
Assistant Clinical Research Coordinator
By UC San Diego Health At , San Diego, 92093, Ca $29.99 - $48.25 an hour
Experience in medical assessment and patient interviewing to determine toxicities related to 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 laboratory procedures and values and experience in interpreting them to determine patient eligibility and potential toxicities.
Experience working with FDA policies regulating clinical trials.
Experience interpreting medical charts, experience in abstracting data from medical records.
Clinical Research Coordinator Assistant
By University of California, San Diego - School of Medicine At San Diego, CA, United States

We are hiring again and would love your help spreading the word. We are looking to fill two Clinical Research Coordinator Assistant positions to contribute to our trials testing neuroimaging-guided ...

Cardiovascular Clinical Research Coordinator (Rn Or Lvn)
By Sharp Community Medical Group At , San Diego, 92123, Ca $37 - $45 an hour
Clinical research: 1 year (Preferred)
Salary: $37.00 - $45.00 per hour
CDHS guidelines are followed. Applicants must be fully vaccinated for Covid-19 by start of employment.
clinical research: 1 year (Preferred)
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.
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 Scheduler Jobs
By UCLA Health At , Los Angeles, 90095 $26.99 - $38.66 an hour

Description Join our team at the Department of Molecular and Medical Pharmacology as a Clinical Research Scheduler and play a vital role in scheduling and coordinating clinical research ...

Clinical Research Analyst Jobs
By Intellectt Inc At Alameda, CA, United States

Position Summary The CRAII/Sr. CRA will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of ...

Assistant Clinical Research Coordinator
By Stanford University At Stanford, CA, United States
Advanced computer skills and demonstrated experience with office software and email applications
General knowledge of medical terminology.
Excellent organizational skills and attention to detail
Strong verbal and written communication skills
Excellent customer service and interpersonal skills
May require extended or unusual work hours based on research requirements and business needs.
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 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 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.
Cancer Clinical Research Coordinator Associate - Hematology
By Stanford University School of Medicine At Stanford, CA, United States
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
Knowledge, Skills And Abilities (required)
Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
Knowledge of the principles of clinical research and federal regulations.
Previous experience with clinical research.
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Program Director, Clinical Research Informatics - Clinical Research
By Keck Medical Center of USC At , Los Angeles, 90015, Ca $158,080 - $260,832 a year
Program Planning and Management - Plans and develops CRI objectives and content. Identify trends and research needs and establish priorities accordingly.
Identify technical education opportunities to enhance user experience.
Develops and manages program budgets and recommends or makes budgetary and resource allocations. Provides financial status reports as requested.
Ensures all information systems products meet standards and user requirements. Tests software and hardware and monitors and resolves problems.
Advises leadership regarding Informatics systems requirements. Facilitates planning and directs the design, installation, modification, and operations of research information systems.
Reviews and prioritizes systems development requests. Prepares cost estimates for current and proposed projects, reflecting staff and equipment requirements.

Are you looking for an exciting opportunity to make a difference in the lives of patients? We are seeking a Clinical Coordinator to join our research team and help us develop innovative treatments for a variety of medical conditions. As a Clinical Coordinator, you will be responsible for coordinating and managing clinical research studies, ensuring compliance with regulatory requirements, and providing support to research staff. If you are passionate about making a difference in the lives of patients, this is the perfect job for you!

Overview Research Clinical Coordinators are responsible for coordinating and managing clinical research projects. They are responsible for ensuring that all research protocols are followed, that data is collected and analyzed correctly, and that the research is conducted in a safe and ethical manner. They may also be responsible for recruiting and training research staff, managing budgets, and ensuring that all regulatory requirements are met. Detailed Job Description Research Clinical Coordinators are responsible for the planning, implementation, and management of clinical research projects. They are responsible for ensuring that all research protocols are followed, that data is collected and analyzed correctly, and that the research is conducted in a safe and ethical manner. They may also be responsible for recruiting and training research staff, managing budgets, and ensuring that all regulatory requirements are met. They must also ensure that all research results are accurately reported and that all research activities are conducted in compliance with applicable laws and regulations. Job Skills Required
• Excellent organizational and communication skills
• Ability to manage multiple projects and tasks simultaneously
• Knowledge of clinical research protocols and procedures
• Knowledge of applicable laws and regulations
• Ability to work independently and as part of a team
• Ability to work with a variety of stakeholders
• Ability to analyze and interpret data
• Knowledge of budgeting and financial management
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research or related field (preferred)
Job Knowledge
• Knowledge of clinical research protocols and procedures
• Knowledge of applicable laws and regulations
• Knowledge of budgeting and financial management
• Knowledge of data analysis and interpretation
Job Experience
• At least two years of experience in clinical research
• Experience in recruiting and training research staff
• Experience in managing research budgets
• Experience in ensuring regulatory compliance
Job Responsibilities
• Plan, implement, and manage clinical research projects
• Ensure that all research protocols are followed
• Collect and analyze data accurately
• Ensure that research is conducted in a safe and ethical manner
• Recruit and train research staff
• Manage research budgets
• Ensure that all regulatory requirements are met
• Report research results accurately
• Ensure that all research activities are conducted in compliance with applicable laws and regulations