Research Project Manager

The incumbent will help manage, plan, and administer the operations of one or more multi-site clinical trial. They will work under Dr. Boxer in a unique position with plenty of room for growth into a high-level administrative and operational position. It requires making decisions using sound judgement, discretion, and professionalism, while working closely and collaborative with other members of the Boxer Lab and external collaborators. The ideal candidate will thrive in a fast-paced environment, possess exceptional organizational skills, and have a passion for contributing to impactful medical research.

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 $78,900 - $167,300 (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

• Bachelor's degree in related area and minimum three years of experience or equivalent experience / training.
• Previous scientific research experience in clinical or laboratory setting
• Strong interpersonal skills including verbal and written communication, active listening, critical thinking, persuasiveness, advising and counseling skills.
• Ability to use discretion and maintain confidentiality.
• Strong skills in short-term planning, analysis, and problem-solving.
• Experience with surveys and presentations including related software (e.g., Smartsheet, Qualtrics, Excel, PowerPoint, etc.)
• Proven ability to work collaboratively with other cross-functional teams and establish cooperative working relationships with co-workers & physicians.
• The ability to work autonomously and conduct oneself in a highly professional manner.

• Thorough knowledge of University rules and regulations, processes, protocols and procedures for budget, accounting and fund management, and / or personnel management.
• Previous experience with human clinical trials
• Knowledge of a variety of administrative operational activities such as risk management planning, accounting and payroll, and contracts and grants regulations and guidelines.
• Solid knowledge of common University-specific computer application programs
• Strong written communication and presentation skills, including writing research protocols, manuscripts, preparing engaging and informative PowerPoint presentations
• Knowledge of ICH guidelines, US FDA, and European clinical trial requirements and regulations