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Clinical Research Scientist I 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 Coordinator I
By Fred Hutch At Seattle, WA, United States
Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently
Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources
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.
Clinical Research Assistant I
By Beth Israel Deaconess Medical Center At , Boston
7. Assists investigator with correspondence with IRB. (essential)
4. Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.
3. Potential exposure to adverse environmental conditions
o Several times a month: Radiation-irradiator possible.
Clinical Research Coordinator I
By Seattle Childrens Hospital At , Seattle, 98105, Wa $55,765 - $83,637 a year
Bachelor's Degree in related discipline, or equivalent combination of education and experience.
Prior experience in research or a related field/setting.
Confirmed proficiency in a second language via successful completion of a language assessment may be required for certain departments.
Min to Max Hourly Salary$26. 81 - $40.21 /hr
Min to Max Annual Salary$55,764.80 - $83,636.80 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Scientist I Jobs
By ImmunityBio, Inc. At Seattle, WA, United States
Excellent skills in prioritizing and time management.
Bachelor’s degree with 10 years’ experience in novel immunotherapies; or
Master’s degree with 8 years’ experience in novel immunotherapies; or
PhD with 2 years’ experience in novel immunotherapies inclusive of postdoc experience
Experience with logistical planning and overseeing the implementation of numerous simultaneous murine experiments.
Possess good interpersonal and strong written/verbal communication skills.
Research Scientist I Jobs
By Seattle Childrens Hospital At , Seattle, 98105, Wa $50,669 - $76,003 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 a challenging and rewarding career in clinical research? We are looking for a Clinical Research Scientist I to join our team and help us develop innovative treatments for a variety of diseases. As a Clinical Research Scientist I, you will be responsible for designing and executing clinical trials, analyzing data, and reporting results. You will also be involved in the development of new therapeutic strategies and the evaluation of existing treatments. If you are passionate about making a difference in the lives of patients, this is the job for you!

Overview Clinical Research Scientist I is a professional who is responsible for conducting clinical research studies and trials. They are responsible for designing, planning, and executing clinical research studies and trials, as well as analyzing and interpreting the data collected. They also provide guidance and support to other clinical research professionals. Detailed Job Description Clinical Research Scientist I is responsible for designing, planning, and executing clinical research studies and trials. They are responsible for developing protocols, collecting and analyzing data, and preparing reports. They also provide guidance and support to other clinical research professionals. They are responsible for ensuring that all clinical research studies and trials are conducted in accordance with applicable regulations and guidelines. Job Skills Required
• Knowledge of clinical research principles and methods
• Knowledge of regulatory requirements and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to analyze and interpret data
• Ability to manage multiple projects simultaneously
• Proficiency in computer applications
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (e.g., CCRA, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research principles and methods
• Knowledge of regulatory requirements and guidelines
• Knowledge of medical terminology
• Knowledge of clinical trial design and implementation
• Knowledge of data analysis and interpretation
Job Experience
• At least two years of experience in clinical research
• Experience in designing, planning, and executing clinical research studies and trials
• Experience in analyzing and interpreting data
• Experience in preparing reports
Job Responsibilities
• Design, plan, and execute clinical research studies and trials
• Develop protocols and collect data
• Analyze and interpret data
• Prepare reports
• Provide guidance and support to other clinical research professionals
• Ensure that all clinical research studies and trials are conducted in accordance with applicable regulations and guidelines