Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Budget Negotiation Analyst - Remote
By UC San Diego Health At , San Diego $75,000 - $95,000 a year
Seven (7) years of related experience, education/training, OR a Bachelor’s degree in related area plus three (3) years of related experience/training.
Thorough knowledge of finance policies, practices, and systems.
Thorough knowledge and understanding of internal control practices and their impact on protecting University resources.
Demonstrated experience analyzing and drafting complex clinical trial budgets and negotiating mutually satisfying terms and conditions.
#122969 Clinical Trial Budget Negotiation Analyst - Remote
Candidates hired into this position may have the ability to work remotely.
Clinical Trial Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
With supervision, assist in the accurate and appropriate study test article management.
Support the effective financial management of the clinical trial.
Other duties as assigned by appropriate management.
Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
Clinical Trial Manager Jobs
By Amgen At Thousand Oaks, CA, United States
Previous managerial experience directly managing people and/or experience in leading teams, projects, programs or directing the allocation of resources
High school diploma/GED and 12 years of Manufacturing & Operations experience OR
Associate’s degree and 10 years of Manufacturing & Operations experience OR
Bachelor’s degree and 5 years of Manufacturing & Operations experience OR
Master’s degree and 3 years of Manufacturing & Operations experience OR
Solid knowledge of downstream, as well as a general knowledge of the associated analytical and buffer preparation techniques
Clinical Trial Rater Jobs
By M3 USA At Los Alamitos, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Manager/Sr. Clinical Trial Manager
By Akero Therapeutics At San Francisco Bay Area, United States
Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
Experience as the regional lead for Europe, United States, and/or India.
Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
This position is for remote work, but may require domestic or international travel as required (valid travel documents must be obtainable).
At least 4+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
Clinical Trial Assistant-1 Jobs
By Cue Health At San Diego, CA, United States
Effective organizational and time management skills; ability to manage multiple assignments and changing priorities
Demonstrate commitment to the implementation and effectiveness of Cue’s Quality Management System
Knowledge of applicable clinical research regulatory requirements (e.g., GCP and ICH GCP)
Create, manage, and audit clinical trial master files and investigator site binders
A minimum of 1 year of experience in clinical research or related field
Previous experience in creating, managing, and auditing clinical trial master files and investigator site binders
Clinical Trial Rater Jobs
By M3 USA At Los Angeles, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Assistant Jobs
By Corcept Therapeutics At Menlo Park, CA, United States
Assist project team with study specific documentation including filing to the Clinical Trial Management System and Trial Master File
Preferred Skills, Qualifications and Technical Proficiencies:
Track clinical supply inventory at sites and manage the site drug re-supply process
Set-up and maintain tracking system with oversight of manager
Develop working knowledge of company standard operating procedures (SOPs) and FDA regulations related to clinical studies
Familiarity with applicable regulatory requirements, Good Clinical Practice/ICH and Good Documentation Practices
Clinical Trial Assistant (Cta)
By Cytokinetics At , South San Francisco, 94080, Ca $31.50 - $38.50 an hour
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant (Cta)
By Cytokinetics At South San Francisco, CA, United States
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant Jobs
By Abbott Laboratories At , San Diego, Ca $24 - $49 an hour
To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
To provide general administrative support to the Clinical Affairs Department and assistance to department Manager(s) and Director(s).
Research or health care related academic or work experience preferable.
Good written and verbal communication skills.
To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.
Clinical Trial Manager Jobs
By 89bio At San Francisco, CA, United States
Experience in CRO selection and management including drafting request for proposals (RFPs), bidding process, etc.
Conduct Site Qualification Visits (SQVs) to assess investigator's staff, capabilities, and facilities
In-depth knowledge of FDA regulatory requirements and medical practice/techniques and terminology
Select and manage vendors (including CROs, central lab, etc.)
Manage investigational product supply at study and site levels
Work with Clinical Research Organizations (CROs) to ensure coordination of Sponsor and CRO responsibilities, obligations are being met
Clinical Trials Navigator Jobs
By UCLA Health At Los Angeles, CA, United States

Please see the link below for more information about this position! Reach out with any questions!

Clinical Nurse Navigator I - Neuroscience Administration
By Hoag Memorial Hospital Presbyterian At , Newport Beach, 92663, Ca $52.77 - $81.74 an hour
Neurosciences: Fulfills mandatory stroke education requirements per certification agency
Minimum of 5 years’ experience in nursing and 3 years’ of experience in area of specialty required.
Additional department specific requirements are as follows:
Registered Nurse in the State of California - Current and in good standing.
Neurosciences (Stroke): AANN (American Association of Neuroscience Nurses): SCRN or CNRN or ANVC (Association of Neurovascular Clinicians): NVRN-BC or ASC-BC
Salary Range: $52.7700 - $81.7400 /hour

Are you looking for an exciting opportunity to make a difference in the lives of patients? Join our team as a Clinical Trial Navigator and help us make a positive impact on the lives of those we serve! As a Clinical Trial Navigator, you will be responsible for providing support and guidance to patients and families throughout the clinical trial process. You will be the go-to person for all questions and concerns related to the trial, and you will ensure that patients are informed and comfortable throughout the process. If you are passionate about helping others and have a strong background in clinical research, this is the perfect job for you!

Overview Clinical Trial Navigators are responsible for providing support and guidance to patients and their families throughout the clinical trial process. They are responsible for helping patients understand the clinical trial process, providing information about the trial, and helping them navigate the various steps of the trial. They also provide support to the clinical trial team by helping to coordinate patient visits, providing patient education, and helping to ensure that the trial is conducted in accordance with the protocol. Detailed Job Description Clinical Trial Navigators are responsible for providing support and guidance to patients and their families throughout the clinical trial process. They are responsible for helping patients understand the clinical trial process, providing information about the trial, and helping them navigate the various steps of the trial. They also provide support to the clinical trial team by helping to coordinate patient visits, providing patient education, and helping to ensure that the trial is conducted in accordance with the protocol. They must be able to communicate effectively with patients, families, and clinical trial staff, and must be able to explain complex medical information in a way that is easy to understand. Clinical Trial Navigators must also be able to work independently and as part of a team. Job Skills Required
• Excellent communication and interpersonal skills
• Ability to explain complex medical information in an easy to understand manner
• Ability to work independently and as part of a team
• Knowledge of clinical trial protocols and procedures
• Knowledge of medical terminology and medical records
• Ability to coordinate patient visits and provide patient education
• Ability to maintain patient confidentiality
• Ability to work with a variety of people from different backgrounds
Job Qualifications
• Bachelor’s degree in a related field such as nursing, health sciences, or social work
• Previous experience in a clinical setting
• Knowledge of clinical trial protocols and procedures
• Knowledge of medical terminology and medical records
• Ability to coordinate patient visits and provide patient education
• Ability to maintain patient confidentiality
• Ability to work with a variety of people from different backgrounds
Job Knowledge
• Knowledge of clinical trial protocols and procedures
• Knowledge of medical terminology and medical records
• Knowledge of patient privacy laws and regulations
• Knowledge of patient rights and responsibilities
• Knowledge of clinical research and clinical trial processes
• Knowledge of patient education and support services
Job Experience
• Previous experience in a clinical setting
• Previous experience working with patients and families
• Previous experience working with clinical trial