Clinical Study Coordinator

2 weeks ago


Los Angeles, California, United States Amerit Consulting Full time
Clinical Study Coordinator Job Description

Amerit Consulting is seeking an accomplished Clinical Study Coordinator to support the regulatory aspect of research projects.

Key Responsibilities:

  • Coordinate clinical trials, data management, and case report forms
  • Support the start-up and closure of clinical research studies
  • Work with multiple investigators on different research projects
  • Ensure compliance with regulatory requirements
  • Collaborate with cross-functional teams to achieve project goals

Requirements:

  • At least 1 year of regulatory coordinator/study coordinator experience
  • Working knowledge of clinical trials, data management, and case report forms
  • ACRP certification preferred
  • Strong interpersonal and communication skills
  • Ability to prioritize effectively and work efficiently

About Amerit Consulting:

Amerit Consulting is a fast-growing staffing and consulting firm providing consulting, temporary staffing, direct hire, and payrolling services to Fortune 500 companies and small to mid-sized organizations.

We develop and implement solutions that help our clients operate more efficiently, deliver greater customer satisfaction, and see a positive impact on their bottom line.

We create value by bringing together the right people to achieve results.

Our clients and employees say they choose to work with Amerit because of how we work with them - with service that exceeds their expectations and a personal commitment to their success.

We provide equal employment opportunities to all employees and applicants for employment and prohibit discrimination and harassment of any type.



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