Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details
Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Bright Research

Study Director

Career Insights for Clinical Research Manager

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Minnesota data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Clinical Research Manager is responsible for managing the day-to-day research operations of an organization undertaking clinical trials, usually pharmacological drug testing.

$166,169 / year median in Minnesota

Explore Career

Job Description

Study Director Bright Research Minneapolis, MN Job Details Full-time $90,000 - $125,000 a year 11 hours ago Benefits Paid parental leave Paid holidays Disability insurance Health insurance On-site gym Dental insurance Tuition reimbursement Parental leave Vision insurance 401(k) matching Qualifications Managing scientific research projects Full Job Description Who are we? Bright Research is a dynamic and growing medical device Clinical Research Organization (CRO) located in downtown Minneapolis. We manage clinical trials from concept to completion, with smarts and sophistication to make the complex look easy. We are seeking a Study Director . This is a position at our downtown Minneapolis office. Who makes an excellent fit for Bright? Are you curious and passionate about MedTech and translating data into clinical stories to advance science? If you have strong communication skills, creativity, resilience and a positive attitude, we would love to hear from you! What does the role require? Serve as the primary sponsor contact, communicate key study updates, and ensure alignment among sponsors, Bright leadership, and study team members. Direct team members on timelines, strategies, and study activities; develop and manage protocols, plans, and study documents; ensure accurate, timely study reporting. Work with sponsors and site personnel to identify, qualify, select, initiate, and train study sites; collaborate with Clinical Research Associate (CRAs) to resolve monitoring findings. Ensure adherence to protocols, Good Clinical Practice (GCPs), regulatory requirements, IRB/EC standards, and internal procedures; identify and mitigate study risks; support audits and inspections. Coordinate with departments such as Data Management and Regulatory; manage activities with third-party vendors (e.g., translation services, core labs); facilitate or assist with investigator, committee, and study team meetings. Provide training and guidance to entry-level team members and participate in staff and project team meetings as needed. Qualifications Education Bachelor's or master's degree in a scientific field, or equivalent work experience Experience At least 5+ years of medical device industry, clinical research experience in a study management or execution role; Management experience preferred Benefits Salary range: $90,000 - $125,000 Complimentary paid parking, comprehensive health insurance (medical, dental, and vision), paid parental leave, short- and long-term disability benefits, a 401(k) with company match, tuition reimbursement, at least 12 paid company holidays, and access to an on-site gym.