Clinical Research Associate I

2 months ago

Los Angeles, California, United States CEDARS-SINAI Full time
About the Role

Cedars-Sinai is seeking a highly skilled Clinical Research Associate I to join our team in the Heart Institute. As a key member of our research team, you will play a critical role in coordinating and implementing clinical studies, ensuring compliance with protocol and research objectives.

Key Responsibilities:

  • Collaborate with research coordinators, administrators, and nurses to coordinate study implementation and data collection.
  • Evaluate and abstract research data from source documents, ensuring accuracy and completeness.
  • Complete case report forms and enter clinical research data into electronic data systems.
  • Provide patient contact and support as needed, ensuring compliance with study protocols and regulations.
  • Assist with regulatory submissions to the Institutional Review Board (IRB), including adverse event reporting and safety letters.
  • Contribute to clinical trial budgets and patient research billing.
  • Schedule patients for research visits and procedures, ensuring timely and efficient study conduct.
  • Prepare and ship study samples, maintaining accurate records and inventory.
  • Ensure compliance with federal and local regulations, including Good Clinical Practice (GCP) guidelines and HIPAA regulations.
  • Participate in required training and education programs to maintain research expertise.
Requirements
  • High school diploma or equivalent required; Bachelor's degree in a related field preferred.
  • At least one year of experience in clinical research or a related field.
About Cedars-Sinai

Cedars-Sinai is a leading academic medical center and a national leader in healthcare innovation. Our mission is to provide high-quality patient care, advance medical research, and educate the next generation of healthcare professionals.

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