Research Compliance Analyst 2 - Urology

$63,565 - $126,006/Yr

University of California - Los Angeles, CA

Full-time - Entry Level

Los Angeles, CA

Educational Services

About the position

UCLA Health is at the forefront of medical research and innovation, and the Department of Urology is seeking a dedicated Research Compliance Analyst II to join our team. This full-time position is pivotal in ensuring the regulatory compliance of clinical research studies within assigned units, departments, or divisions. As a Research Compliance Analyst II, you will be responsible for the regulatory coordination of clinical research studies, which includes performing detailed reviews of clinical research protocols. You will utilize this information to prepare, manage, and submit all required study and regulatory documents, as well as all necessary applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, and more. In this role, you will work closely with study monitors to process, review, and collect the appropriate regulatory documents in a timely manner, ensuring compliance with federal, state, and university mandated laws, regulations, and policies. Your attention to detail and organizational skills will be crucial as you navigate the complexities of clinical research compliance. At UCLA Health, we are committed to making a difference in the lives of people around the world through our passion for discovery and innovative therapies. If you are looking for a challenging and fulfilling career in a dynamic environment, we invite you to apply and contribute to our mission of redefining human health and patient care.

Responsibilities

• Perform detailed reviews of clinical research protocols.
• Prepare, manage, and submit all required study and regulatory documents.
• Ensure compliance with internal UCLA requirements, FDA requirements, and sponsor requirements.
• Work with study monitors to process, review, and collect appropriate regulatory documents.
• Maintain administrative and regulatory files effectively.
• Set priorities and complete ongoing tasks with competing deadlines.

Requirements

• 1+ years of clinical research experience.
• High school diploma or GED.
• Interpersonal skills to communicate effectively and maintain cooperative relationships.
• Ability to set priorities and complete tasks with competing deadlines.
• Analytical skills to assess clinical research protocols and regulatory requirements.
• Close attention to detail to ensure accuracy in a fast-paced environment.
• Organizational skills to create and maintain files and balance various tasks.
• Proficiency with Adobe and Microsoft Office Suite, especially Excel.
• Knowledge of clinical research concepts, policies, and procedures.

Nice-to-haves

• Associate's or Bachelor's Degree.