Clinical Data Coordinator

If you are passionate about data management and have a strong interest in clinical research, we encourage you to apply for the position of Clinical Data Coordinator

Job Title: Clinical Data Coordinator

Location: San Francisco, California, United States

Salary: $69 Per hour

Position Overview: We are seeking a highly organized and detail-oriented individual to join our team as a Clinical Data Coordinator. In this role, you will be responsible for managing and maintaining all aspects of clinical data, ensuring accuracy and completeness, and providing support to the clinical research team. The ideal candidate will have excellent analytical skills, a strong understanding of data management principles, and experience working in a clinical research environment.

Key Responsibilities:

• Collect and maintain accurate and complete clinical data in accordance with study protocols and applicable regulations
• Review and verify data for completeness, accuracy, and consistency
• Identify and resolve data discrepancies and issues in a timely manner
• Develop and maintain data management plans and data collection tools
• Coordinate with clinical research staff to ensure data is entered and managed accurately and efficiently
• Generate and distribute reports on data quality and completeness for internal and external stakeholders
• Conduct data cleaning and data validation activities
• Ensure compliance with regulatory requirements and company policies related to data management
• Train and provide guidance to clinical research staff on data management processes and procedures
• Participate in the development and implementation of standard operating procedures (SOPs) for data management
• Collaborate with cross-functional teams to identify areas for process improvement and implement solutions
• Maintain up-to-date knowledge of industry standards and best practices for data management

Qualifications:

• Bachelor���s degree in a relevant field, such as health sciences, statistics, or data management
• Minimum of 2 years of experience in data management, preferably in a clinical research setting
• Strong understanding of FDA regulations, ICH guidelines, and GCP principles
• Proficiency in data management software and tools, such as EDC systems and databases
• Excellent attention to detail and ability to work with complex data sets
• Strong analytical and problem-solving skills
• Ability to work independently and manage multiple tasks with competing priorities
• Excellent communication and interpersonal skills
• Experience with clinical data management systems, such as Medidata Rave or Oracle Inform, is preferred
• Knowledge of programming languages, such as SQL or SAS, is a plus

Working Conditions: This is a full-time position, based in our office. Occasional travel may be required to attend conferences or training sessions.

We offer a competitive salary and benefits package, as well as opportunities for professional development and growth within the company.

We are looking for a dedicated and motivated team player to join our dynamic and innovative organization.