Regulatory Project Manager - Hematology/Oncology (Fully Remote)
UCLA HealthAbout the role
General Information
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Primary Duties and Responsibilities
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We are seeking an experienced Regulatory Project Manager who will be responsible for regulatory coordination of complex clinical research studies within assigned units, departments or divisions. In this role, you will perform detailed review of clinical research protocols and utilize that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc. Additionally, you will work with study monitors to process, review and collect the appropriate regulatory documents in a timely manner and in compliance with federal, state, and university mandated laws, regulations and policies.
Annual Salary Range: $78,500.00 - $163,600.00. Please note, the department’s target salary range is $78,500.00 - $121,000.00
Job Qualifications
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Required:
- Minimum of 3+ years of experience of clinical research coordination
- Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.
- Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.
- Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
- Close attention to detail to ensure accuracy in a fast-paced, fluctua
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