Research Lab Assistant

Starkey Canada•Eden Prairie, MN

3d•$20 - $28•Onsite

About The Position

Starkey is adding a Research Lab Assistant at its global headquarters in Eden Prairie, MN. The Research Lab Assistant supports the successful execution of clinical research studies by ensuring efficient study operations, accurate documentation, and well-maintained lab environments. This role blends administrative, technical, and operational responsibilities and is ideal for someone who is highly organized, detail-oriented, and comfortable managing multiple priorities in a regulated research setting. Starkey is a world leader in the manufacturing and distribution of advanced hearing technologies. We are in the business of connecting people and changing lives. Our teams come to work each day focused on ensuring people everywhere have the products and services they need to hear better and live better. Founded in 1967 by Bill Austin, Starkey is known for our cutting-edge hearing health innovations, industry-leading research and development, and not being afraid to push the edge of what’s possible. We are headquartered in Eden Prairie, Minnesota, have over 5,000 employees in 29 facilities across the globe, and do business in more than 100 markets worldwide. Watch this video to see more of what sets Starkey apart. https://youtu.be/9cUYwTlCepg?si=wkovx8_R_iINfrc6

Requirements

Associate’s or Bachelor’s degree in a related field (e.g., Life Sciences, Health Sciences, Biomedical Engineering, or similar) preferred
0–2 years of experience in a laboratory, clinical research, healthcare, or healthcare environments
Internship, academic lab, or hands-on project experience is highly valued
Familiarity with regulatory requirements (e.g., documentation)
Experience with data management systems or research tools
Hearing Instrument Specialist (HIS) certification or willingness to obtain
Experience with hearing impaired patients preferred
Basic understanding of clinical research processes and regulated environments (e.g., documentation standards, data integrity)
Familiarity with data entry systems, spreadsheets (e.g., Excel), and database tools
Experience with participant recruitment and scheduling preferred
Ability to learn and utilize clinical and engineering software/tools for data export and analysis
Understanding of general lab practices, equipment handling, and safety procedures
Knowledge of Good Clinical Practice (GCP) principles or willingness to learn
Exposure to regulatory requirements related to adverse event reporting and study documentation (preferred)
Basic technical aptitude for preparing and testing devices, including data checks and measurements
Attention to Detail: Ensures accuracy and completeness in documentation, data entry, and reporting
Organization & Time Management: Effectively manages multiple priorities while maintaining structured systems
Accountability: Takes ownership of tasks and follows through on commitments in a timely manner
Adaptability: Learns quickly and adjusts to changing study needs, tools, and processes
Collaboration: Works effectively with cross-functional teams including research, engineering, and clinical staff
Communication: Clearly communicates status, issues, and updates to team members and stakeholders
Problem Solving: Identifies issues and takes initiative to resolve them or escalate appropriately

Nice To Haves

Hearing Instrument Specialist (HIS) certification or willingness to obtain
Experience with hearing impaired patients preferred
Experience with participant recruitment and scheduling preferred
Knowledge of Good Clinical Practice (GCP) principles or willingness to learn
Exposure to regulatory requirements related to adverse event reporting and study documentation (preferred)

Responsibilities

Manage study documentation, including electronic storage of consent forms, database entry, and maintenance of organized study records
Oversee lab supply inventory, track stock levels, and coordinate ordering through approved procurement channels
Prepare study materials, including assembling binders, printing documents, and organizing participant supplies and paperwork
Maintain lab spaces to ensure cleanliness, organization, and readiness for active and upcoming studies
Perform data entry and support data management activities to ensure accuracy, completeness, and compliance
Export and organize study data for engineering teams using clinical and technical tools
Complete documentation in accordance with regulatory and study-specific requirements
Prepare devices for study use, including test box measurements, data exports, and listening checks
Support hearing evaluations as a Hearing Instrument Specialist (HIS), if trained and interested
Organize and attach raw data to validation reports in alignment with regulatory standards
Perform other duties/responsibilities as assigned