Why This Role Stands Out
This hybrid User Study Operations Manager role offers exciting opportunities to manage global research projects for a leading consumer device company, developing crucial skills in vendor management and cross-functional collaboration. You will thrive here if you are a proactive, mid-senior professional with at least three years of relevant experience, eager to drive impactful projects and contribute to innovative product development. Apply now to gain valuable experience and advance your career in a dynamic, globally recognized organization with competitive hourly compensation.
Quick Overview
Job Description
A globally leading consumer device company based in Sunnyvale, CA is looking for
Responsibilities:
Lead communication between project teams and external vendors
Develop enrollment and throughput plans
Manage and communicate project status with cross-functional teams and external vendors
Drive project scoping with research vendors including quotes, contracts, budget management, and invoicing
Deliver high quality, low cost results
Proactively, Identify and resolve risks to schedule and data quality
Balance multiple projects across geographic regions throughout the globe
Initiate, execute, and report status with keen focus on data quality and schedule
Develop study documents like consent forms, statements of work, and SOPs
Order, coordinate, and distribute study supplies to researchers inclusive of device set-up as needed
Facilitate communication and collaboration across a very multi-functional team including: engineering, studies, design teams, clinical, and regulatory
Develop and train study personnel on data collection procedures, use of study systems and data monitoring processes
Key Qualifications:
Minimum 3+ years of experience in health research management, engineering operations, or relevant medical / clinical experience.
Demonstrated ability to execute engineering research projects of varying sizes
Troubleshoots hardware and software challenges, analyzes engineering data to make study-level recommendations
Thrives by managing fast paced projects with minimal direction
Excellent written and verbal communication skills
Track record of managing vendors or contractors to deliver timely results
Experience with clinical and/or medical device research
Facilitated communication and collaboration across a very multi-functional team including: engineering, studies, design teams, clinical, and regulatory
BA/BS or higher in biomedical engineering, life sciences, or research-related discipline.
Must have 2+ years of experience directly supporting technical operations in a research setting. Advanced degree or experience analyzing engineering data is a plus, but not required.
Type: Contract
Duration: 12 months with extension
Work Location: Sunnyvale, CA (hybrid)
Pay range: $56.00 - $71.00/hr (DOE)
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