User Study Researcher I
Apply NowCompany: WinMax Systems Corporation
Location: Cupertino, CA 95014
Description:
Title:User Study Researcher I, Req# 33854988
Location: Cupertino,CA(Hybrid)
Contract: 12+ Month
Job Description:
Key Qualifications
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
Description
Responsibilities include:
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
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
Develop and train study personnel on data collection procedures, use of study systems and data monitoring processes
Education & Experience
BA/BS or higher in biomedical engineering, life sciences, or research-related discipline.
Minimum 3+ years of experience in health research management, engineering operations, or relevant medical / clinical experience.
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.
PayRate :$60-69/hr,w2
Location: Cupertino,CA(Hybrid)
Contract: 12+ Month
Job Description:
Key Qualifications
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
Description
Responsibilities include:
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
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
Develop and train study personnel on data collection procedures, use of study systems and data monitoring processes
Education & Experience
BA/BS or higher in biomedical engineering, life sciences, or research-related discipline.
Minimum 3+ years of experience in health research management, engineering operations, or relevant medical / clinical experience.
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.
PayRate :$60-69/hr,w2