Clinical Study Coordinator - Part Time

General Information

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Work Location: Long Beach, USA Onsite or Remote Fully On-Site Work Schedule Monday- Friday 8am-5pm Posted Date 10/02/2024 Salary Range: $33.63 - 54.11 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 19469

Primary Duties and Responsibilities

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We are excited to invite applications for the role of Clinical Research Coordinator in the UCLA Division of Digestive Diseases. We seek a highly motivated, dynamic, and detail-oriented individual to join our dedicated team.

As a Clinical Research Coordinator, you will play a vital role in the operational management of clinical research and study activities, overseeing projects from design and setup to conduct and closeout. This position will primarily focus on funded projects related to esophageal cancer, offering an incredible opportunity to learn from patients and contribute to improving overall care.

Key Responsibilities:

• Implement research activities for one or more studies, ensuring adherence to study protocols and applicable regulations, including institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).
  
• Manage project tasks effectively, prioritizing work to meet deadlines and ensure compliance.
  
• Collaborate with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, and other entities to support all aspects of the studies, including compliant conduct, financial management, and personnel support.
  

Join us at UCLA Health, where you will have the opportunity to make a meaningful impact on clinical research and patient care. We look forward to your application!

This is a 50% part- time position

Salary: $33.63 - $54.11 hourly

Job Qualifications

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Required: 

• Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
  
• Working knowledge of the clinical research regulatory framework and institutional requirements.
  
• Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
  
• Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
  
• Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
  
• Analytical