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Clinical Study Coordinator Jobs in California

Clinical Study Assistant Jobs
By Kelly Science, Engineering, Technology & Telecom At Irvine, CA, United States
Run reports including training matrix reports, metrics for management reviews
Support management of IRB/IEC renewal compliance.
Work with management group to help achieve department goals.
Requires experience and knowledge working with computer systems (Microsoft office –
Assist in payments/tracking for patient reimbursements. Performs data entry in systems
Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
Study Coordinator Jobs
By RootStaff At San Rafael, CA, United States
Relevant administrative experience including detail oriented, collaborative, positive attitude, ability to prioritize, proactive, and good follow up skills,
Administrative tasks and activities may be requested by a line manager, study team member, or GSO department staff.
Assist with tracking and review of Clinical Trial Insurance requirements, expiry dates, insurance renewal, certificate distribution, and archival
Activities and responsibilities may include:
The SS I is not allocated as a resource to any specific study or program.
BOARD Quarterly MVR GSO Compliance and other metrics
Part-Time Contract Clinical Study Coordinator
By NeuroPace At San Francisco Bay Area, United States
General understanding of clinical documentation management and document control
Manage the eTMF (Trial Master File) system
Minimum of 2 years relevant work experience
Medidata and eTMF experience preferred
Previous experience in a clinical or regulatory department highly preferred.
Proficient in MS Word, Excel and Adobe PDF. Experience with clinical trial software systems, including eTMF, preferable
Clinical Study Coordinator (Remote)
By Guardant Health At Palo Alto, CA, United States
Facilitate the coordination and management of clinical studies
Knowledge of ICH/GCP guidelines, including basic understanding of regulatory requirements in other countries, preferred
A minimum of 1 year experience in a CLIA, CAP-accredited laboratory preferred
A minimum of 1 year of experience as a clinical research coordinator preferred, ideally in a lab or device setting
Working knowledge of local, state, and federal laboratory regulations
Effective interpersonal skills and ability to effectively communicate (verbal and written) across all levels of the company
Study Coordinator Jobs
By UCLA Health At Santa Monica, CA, United States
- 1+ years of experience within clinical research
- Bachelors Degree in related field
- Ability to handle a high volume of trials at a given time
- Oncology clinical research background

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