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Clinical Research Trials Coordinator Jobs in San Mateo, California

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 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 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 ...

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.
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
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.
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 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 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 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.
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 I, Strive & Bhs
By Tulane University At , Bogalusa, La
Strong communication skills both verbal and written, report writing, and ability to meet deadlines
Good team member and experience in working in an office environment
LPN with current state licensure at the time of hire and three (3) years of related work experience
Experience working on a research study or clinic is preferred, but not required
Experienced with research coordination and teams
Ability to acquire and maintain all required CITI training certificates
Senior Clinical Research Coordinator
By Velocity Clinical Research, Inc. At Huntington Park, CA, United States
Mentor and train staff in the conduct of clinical trials, protocol requirements, communication, and trial management skills
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.
Advanced knowledge of medical terminology
Advanced verbal, written, and organizational skills
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 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
Assistant Clinical Research Coordinator (1 Year Fixed-Term)
By Stanford University At Stanford, CA, United States
Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
Prepare, process, and ship specimens/samples accurately under well-defined requirements.
May require extended or unusual work hours based on research requirements and business needs.
Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
Prepare, distribute, and process questionnaires.
Extract data from source documents for research studies as directed. Collect data and complete case report forms.

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