Clinical Research Specialist, (Irvine)- Thv
By Edwards Lifesciences At Irvine, CA, United States
Experience in clinical site monitoring, site qualification, and site educational training
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
Experience in Medical device trial
Dps Clinical Research Assistant I - Outcomes Research
By City of Hope At Duarte, CA, United States
Experience may substitute for minimum education requirements
Basic education, experience and skills required for consideration:
Preferred education experience and skills:
Conducts protocol management for an assigned set of multiple research protocols.
Performs data management and data analyses, as required by the research study.
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 ...

Clinical Research Specialist Jobs
By Mindlance At Irvine, CA, United States
• Demonstrated experience in establishing and maintaining effective relationships with management, peers and subordinates and customers.
5) What are the top 5 skills/requirements this person is required have?
• Manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges.
a. Required Skill 1: Organized and great attention to detail
b. Required Skill 2: Strong communication skills and intrapersonal skills
c. Required Skill 3: Takes initiative and works well alone and also within a team
Clinical Research Project Manager
By Proper Career Solutions At Los Angeles, CA, United States
• MT Group is a CRO for biospecimen sample acquisition and management
1+ years experience in any of the following:
• 2+ years of experience in a science, research, or medical setting
• Full Benefits (Medical, Vision)
As a research coordinator or research associate
• Small, Growing Company (30 people)
Clinical Research Project Manager
By Crowdstaffing powered by Prosperix At South San Francisco, CA, United States
Bachelor's degree or equivalent practical experience. 3-5 years of experience working in project management or similar discipline.
Strong working knowledge of project management tools such as spreadsheets, Google Docs, and Project tracking software.
Knowledge and experience of clinical trials.
Excellent communication skills, with experience in communication with executives.
Proven ability to manage complex projects involving multiple stakeholders, and in a fast pace environment.
Strong problem-solving and analytical skills, and ability to handle ambiguity and create order out of it.
Clinical Research Specialist, (Hybrid, Irvine)- Tmtt
By Edwards Lifesciences At Irvine, CA, United States
Experience in site monitoring/central monitoring skills, site qualification, and site training
Data management experience or analytics
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
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.
Clinical Research Assistant Jobs
By UCLA Health At , Santa Monica, Ca $18.06 - $35.78 an hour

Description Join our team as a Clinical Research Assistant and participate in all research activities as part of the clinical research team located at UCLA/UCLA Santa Monica and Westwood while ...

Clinical Research Scientist Jobs
By Johnson & Johnson At Milpitas, CA, United States
Represent Clinical Science in cross-functional project team meetings, provide project team requirements as needed, with input/guidance from senior function members.
Align with Clinical Operations team (study managers, CRAs) on project status/updates and identify issues or impact to project timelines as appropriate.
At least 6 years of work experience
Experience in clinical or scientific research
Experience in class III medical device research
Solid understanding of industry regulatory and compliance requirements
Clinical Research Manager Jobs
By Stanford University School of Medicine At Stanford, CA, United States
Knowledge, Skills And Abilities (required)
Experience developing reports and dashboards
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
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.
Supervise the implementation of and adherence to study protocols. Educate research staff on established policies, processes, and procedures.
Clinical Research Jobs
By Intellectt Inc At Alameda, CA, United States
Role: Clinical Research Associate (CRA) - B
Location: Alameda, CA - 94502
Duration: Long-Term Months on W2
• Minimum of 3 to 5 years of clinical exp. within industry
• Specifically looking for monitoring exp. on the sponsor side
• Will be supporting a multi-site study

Are you looking for a career that combines your passion for science with the opportunity to make a real difference in people's lives? Join our team as a Clinical Research Associate and help us develop treatments that will improve the lives of patients around the world!

Overview of Clinical Research Clinical research is a field of healthcare science that focuses on the evaluation of new medical treatments, drugs, and devices. Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. Detailed Job Description of Clinical Research Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. They must ensure that all research is conducted in accordance with ethical and legal standards. Clinical research professionals must also be able to communicate effectively with other healthcare professionals, patients, and sponsors. Clinical Research Job Skills Required
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Ability to analyze and interpret data
• Ability to communicate effectively
• Ability to work independently
• Attention to detail
• Problem-solving skills
• Computer skills
Clinical Research Job Qualifications
• Bachelor’s degree in a related field
• Master’s degree in a related field
• Certification in clinical research
• Experience in clinical research
Clinical Research Job Knowledge
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Knowledge of clinical research regulations
• Knowledge of data analysis techniques
Clinical Research Job Experience
• Experience in clinical research
• Experience in data analysis
• Experience in project management
• Experience in report writing
Clinical Research Job Responsibilities
• Design and conduct clinical trials
• Collect and analyze data
• Report results
• Ensure compliance with ethical and legal standards
• Communicate effectively with other healthcare professionals, patients, and sponsors
• Monitor patient safety during clinical trials
• Prepare and submit reports to regulatory agencies