Clinical Research Analyst

University of California System • San Francisco, CA

42d • $104,000 - $156,300

About The Position

The Loewy (JJBH) lab is seeking a Clinical Research Analyst to assist with complex tasks within the research lab. Duties include the development of and ensuring compliance with clinical study protocols that involve human subjects. The candidate will oversee and resolve operational aspects of clinical studies or trials in conjunction with project teams and in accordance with standard operating procedures and good clinical practice and regulations. The candidate will collaborate with investigative teams at several other universities, as well as a large number of sites throughout the U.S. The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. The salary range for this position is $104,000 - $156,300 (Annual Rate). To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

Requirements

• Bachelor's degree in related area and minimum five years of experience or equivalent experience / training
• Advanced knowledge of clinical research practices and philosophy, and ability to apply knowledge and skills to recommend improvements in methodology. Advanced knowledge of regulatory requirements
• Advanced ability to effectively lead one or more projects with competing to meet the demands of a fast-paced and dynamic work environment. Adaptable to quickly changing priorities
• In depth critical thinking skills to evaluate issues and identify a potential solution. Creatively addresses complex or new problems
• Advanced communication skills; including verbal and written, active listening, critical thinking, persuasiveness, advising and counseling skills. Clear and concise communicator
• Advanced interpersonal skills, including but not limited to: problem-solving, teamwork development, leadership with other team members. Works well with others to achieve common goals
• Proven ability to perform all commonly applicable functions in word processing and spreadsheet software. Advanced knowledge of clinical information and documentation application programs. Proven ability utilizing clinical trial management systems
• In depth ability to work collaboratively with other cross-functional teams. In depth ability to interface, collaborate and influence / persuade other members of an extended study team

Nice To Haves

• Possession of an advanced degree such as an M.A., Ph.D. or Psy.D
• Early psychosis fidelity and program development experience

Responsibilities

• Development of and ensuring compliance with clinical study protocols that involve human subjects.
• Oversee and resolve operational aspects of clinical studies or trials in conjunction with project teams and in accordance with standard operating procedures and good clinical practice and regulations.
• Collaborate with investigative teams at several other universities, as well as a large number of sites throughout the U.S.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Educational Services
• Number of Employees: 5,001-10,000 employees