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Initiation Clinical Research Associate Ii Jobs in Washington

Clinical Research Coordinator I/Ii
By Fred Hutch At Seattle, WA, United States
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
Knowledge of clinical trials records, procedures, and computerized data processing systems. Demonstrated knowledge of how to synthesize study conduct.
Clinical Research Assistant Ii - Leukemia Research In Ccto
By Beth Israel Deaconess Medical Center At , Boston
1-3 years of related work experience in a medical setting and/or in clinical research required.
Working knowledge of computerized data required including word processing, spreadsheets and databases.
Independence of Action: Ability to follow general instructions and procedures as provided. Work is monitored by supervisor/manager.
Checks all eligibility and ineligibility criteria with patients' medical record. Verifies information with clinical research nurse and/or principal investigator.
Bachelor's degree required; Master's degree preferred.
Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.
Research Associate Ii, Core Technologies, Cell Analytics
By Astellas Pharma US At Seattle, WA, United States
Strong organizational, time management skills, and the ability to maintain accurate and up-to-date records.
Excellent communication and interpersonal skills.
Experience with pluripotent stem cell culture techniques.
Experience performing assays within a Quality Assurance framework
Experience designing, troubleshooting, and optimizing cell-based assays
$64,500 – $86k (NOTE: Final salary could be more or less, based on experience)
Clinical Research Coordinator Ii
By Seattle Childrens Hospital At , Seattle, 98105, Wa $67,454 - $101,192 a year
Min to Max Hourly Salary
Min to Max Annual Salary
The union pay ranges can be found on the Seattle Children's website here: WSNA - UFCW
Disclaimer for Out of State Applicants
Seattle Children's is proud to be an Equal Opportunity Workplace and Affirmative Action Employer.

Are you looking for an exciting opportunity to join a dynamic team of Clinical Research Associates and help shape the future of medical research? We are looking for a Clinical Research Associate II to join our team and help us make a difference in the lives of patients. As a Clinical Research Associate II, you will be responsible for the initiation, monitoring, and close-out of clinical trials. You will also be responsible for ensuring compliance with applicable regulations and guidelines. If you are a motivated individual with a passion for clinical research, this may be the perfect opportunity for you!

Overview The Initiation Clinical Research Associate II is responsible for the initiation and management of clinical research studies. This role requires a high level of knowledge and experience in clinical research and the ability to effectively manage multiple projects. Detailed Job Description The Initiation Clinical Research Associate II is responsible for the initiation and management of clinical research studies. This includes developing and executing study protocols, managing study budgets, and ensuring compliance with applicable regulations and guidelines. The Initiation Clinical Research Associate II is also responsible for coordinating and managing the activities of the study team, including the clinical research staff, investigators, and other stakeholders. Job Skills Required
• Knowledge of clinical research principles and practices
• Knowledge of applicable regulations and guidelines
• Excellent organizational and project management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to manage multiple projects simultaneously
Job Qualifications
• Bachelor’s degree in a related field
• At least 3 years of experience in clinical research
• Certification in clinical research (e.g. CCRA, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research principles and practices
• Knowledge of applicable regulations and guidelines
• Knowledge of clinical trial design and data management
• Knowledge of Good Clinical Practice (GCP)
Job Experience
• At least 3 years of experience in clinical research
• Experience in managing clinical research studies
• Experience in coordinating and managing the activities of the study team
Job Responsibilities
• Develop and execute study protocols
• Manage study budgets
• Ensure compliance with applicable regulations and guidelines
• Coordinate and manage the activities of the study team
• Monitor study progress and ensure data accuracy
• Prepare and submit study reports
• Provide training and guidance to study team members