Brio Group
Senior Clinical Research Specialist
We’re looking for an experienced
Senior Clinical Research Specialist
to join a growing medical device organization in the Twin Cities metro, focused on advancing patient care through innovative clinical research.
In this role, you’ll take ownership of
global clinical studies
across all phases — from feasibility through post-market. You’ll collaborate cross-functionally with regulatory, product development, and marketing teams to ensure studies are executed with precision and integrity.
Responsibilities
Lead development of study protocols, case report forms, and other clinical documents
Coordinate and monitor clinical trial execution at global sites
Partner with regulatory agencies and CROs to support trial success
Oversee budgets, timelines, and data quality for multiple studies
Prepare clinical reports and present outcomes to senior leadership
Requirements
Bachelor’s degree in a scientific or health-related discipline
5+ years of clinical research experience in the medical device industry
Proven success managing clinical trials and leading cross-functional teams
Strong understanding of GCP, SOPs, and regulatory standards
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Senior Clinical Research Specialist
to join a growing medical device organization in the Twin Cities metro, focused on advancing patient care through innovative clinical research.
In this role, you’ll take ownership of
global clinical studies
across all phases — from feasibility through post-market. You’ll collaborate cross-functionally with regulatory, product development, and marketing teams to ensure studies are executed with precision and integrity.
Responsibilities
Lead development of study protocols, case report forms, and other clinical documents
Coordinate and monitor clinical trial execution at global sites
Partner with regulatory agencies and CROs to support trial success
Oversee budgets, timelines, and data quality for multiple studies
Prepare clinical reports and present outcomes to senior leadership
Requirements
Bachelor’s degree in a scientific or health-related discipline
5+ years of clinical research experience in the medical device industry
Proven success managing clinical trials and leading cross-functional teams
Strong understanding of GCP, SOPs, and regulatory standards
#J-18808-Ljbffr