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Clinical Research Trials 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 ...

Research Associate Ii / Lvn, San Diego Clinical Trials (Durational W/Benefits)
By Kaiser Permanente At , San Diego $63,500 - $82,060 a year
Must be able to work in a Labor/Management Partnership environment.
Adheres to compliance and privacy/ confidentiality requirements and standards. Adheres to GCP and compliance regulations for clinical trials.
Acquires and maintains knowledge of KP systems and databases.
Minimum one (1) year of experience coordinating research projects under specific guidance.
Minimum one (1) year of training and/or experience in research methodology/research study design, hypothesis testing; OR
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR
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 Trials Manager Jobs
By Topcon Healthcare At La Jolla, CA, United States
Adverse Event Management: Assist in the identification and reporting of adverse events and ensure that they are handled appropriately
5+ years of experience managing clinical trials in a medical device or pharmaceutical company
Strong knowledge of FDA regulations and GCP guidelines
Excellent communication and interpersonal skills
Ability to manage multiple priorities and work effectively in a fast-paced environment
Experience with managing study budgets and timelines
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.
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 Trials Data Coordinator - Remote
By City of Hope At Duarte, CA, United States
Basic education, experience and skills required for consideration:
Data Management & Protocol Compliance
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, and IRB requirements.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
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 Associate I - Clinical Trials Office
By Cedars-Sinai At West Hollywood, CA, United States
Participates in required training and education programs
1 year Clinical Research Related Experience preferred
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are looking for a Clinical Research Trials Coordinator to join our team and help us develop and execute clinical trials for our cutting-edge medical products. As a Clinical Research Trials Coordinator, you will be responsible for coordinating all aspects of clinical trials, from protocol development to data collection and analysis. You will also be responsible for ensuring compliance with all applicable regulations and guidelines. If you are a detail-oriented professional with a passion for clinical research, this is the perfect job for you!

Overview:

A Clinical Research Trials Coordinator is responsible for coordinating and managing clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations.

Detailed Job Description:

Clinical Research Trials Coordinators are responsible for the planning, implementation, and management of clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations. They must also coordinate with other members of the research team, such as physicians, nurses, and other healthcare professionals. Clinical Research Trials Coordinators must be able to effectively communicate with participants and other members of the research team. They must also be able to interpret and analyze data, and provide feedback to the research team.

What is Clinical Research Trials Coordinator Job Skills Required?

• Excellent communication and interpersonal skills
• Strong organizational and time management skills
• Ability to interpret and analyze data
• Knowledge of applicable regulations and guidelines
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

What is Clinical Research Trials Coordinator Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (optional)

What is Clinical Research Trials Coordinator Job Knowledge?

• Knowledge of clinical research protocols and procedures
• Knowledge of applicable regulations and guidelines
• Knowledge of data collection and analysis
• Knowledge of medical terminology

What is Clinical Research Trials Coordinator Job Experience?

• Experience in clinical research
• Experience in data collection and analysis
• Experience in recruiting and enrolling participants

What is Clinical Research Trials Coordinator Job Responsibilities?

• Recruit and enroll participants for clinical research trials
• Collect and manage data for clinical research trials
• Ensure compliance with all applicable regulations and guidelines
• Coordinate with other members of the research team
• Interpret and analyze data
• Provide feedback to the research team