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Clinical Study Coordinator Jobs in Washington

Research Study Coordinator Jobs
By University of Washington At Seattle, WA, United States
Demonstrated experience in grant preparation, contract management, and IRB protocol development/adherence;
Strong organizational and time management skills with ability to lead research projects;
A Bachelor's degree in a relevant academic area AND two years of experience as a Research Study Coordinator DESIRED QUALIFICATIONS
Other miscellaneous administrative support. MINIMUM REQUIREMENTS
Experience in the preparation of academic manuscripts, posters, and presentations;
Excellent verbal and written communication skills including the ability to communicate via email effectively and efficiently; the ability to work independently;
Research Study Coordinator (Fixed Duration/Temporary)
By University of Washington At , Seattle, 98195, Wa $3,260 - $4,239 a month
Assist in preparation of manuscripts for publication using current American Psychological Association style requirements.
Manage inventory, order supplies, print advertising and study materials, and maintain up-to-date budget documentation with oversight.
one year duration full time research study coordinator
Work as a part of an active and collegial investigative team, demonstrating clear, collegial, and professional communication.
Assist in modifying data collection materials forms using Qualtrics or other online collection platforms.
Assist key personnel to complete reports to various regulatory agencies.
Research Study Coordinator 1 Jobs
By University of Washington At , Seattle, 98195, Wa $3,260 - $4,239 a month
Maintains data collection files and provides support for data management (10%)
Previous experience developing study materials for individuals with disabilities AND recruiting individuals with disabilities
Good working knowledge of Microsoft Office suite and Windows OS
Previous experience involving information collected form research with human subjects and/or observational data
50% FTE (20 hours/week). The shift is flexible, including the possibility of remote work.
Note: This is a 50% FTE position.

Are you looking for an exciting opportunity to be part of a dynamic clinical research team? We are seeking a Clinical Study Coordinator to join our team and help us make a difference in the lives of patients. As a Clinical Study Coordinator, you will be responsible for managing clinical studies from start to finish, ensuring that all study protocols are followed and that data is collected and reported accurately. If you are a detail-oriented individual with excellent organizational skills, this could be the perfect job for you!

Overview Clinical Study Coordinators are responsible for managing the day-to-day operations of clinical research studies. They are responsible for ensuring that all study protocols are followed, that data is collected accurately, and that the study is conducted in compliance with all applicable regulations. Detailed Job Description Clinical Study Coordinators are responsible for the overall management of clinical research studies. This includes developing and implementing study protocols, recruiting and enrolling study participants, collecting and managing study data, and ensuring that all study activities are conducted in compliance with applicable regulations. Clinical Study Coordinators also provide support to the study team, including physicians, nurses, and other healthcare professionals. Job Skills Required
• Strong organizational and communication skills
• Knowledge of clinical research protocols and regulations
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office and other computer applications
• Ability to manage multiple tasks and prioritize work
• Attention to detail
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical research or healthcare
• Certification in clinical research (e.g., CCRC, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of data management systems
Job Experience
• Previous experience in clinical research or healthcare
• Experience in data collection and management
• Experience in recruiting and enrolling study participants
Job Responsibilities
• Develop and implement study protocols
• Recruit and enroll study participants
• Collect and manage study data
• Ensure compliance with applicable regulations
• Provide support to the study team
• Monitor study progress and report any issues
• Prepare study reports and presentations