SonicJobs Logo
Left arrow iconBack to search

Study Director

BRIGHT RESEARCH PARTNERS INC
Posted a month ago, valid for 13 days
Location

Minneapolis, MN, US

Salary

$90,000 - $125,000 per year

Contract type

Full Time

Health Insurance
Tuition Reimbursement

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • Bright Research, a medical device Clinical Research Organization located in downtown Minneapolis, is seeking a Study Director.
  • The ideal candidate should possess at least 5 years of experience in the medical device industry, specifically in clinical research and study management.
  • Responsibilities include serving as the primary contact for sponsors, managing study protocols, and ensuring compliance with regulatory standards.
  • The position offers a salary range of $90,000 to $125,000, along with a comprehensive benefits package including health insurance and paid parental leave.
  • Candidates should have strong communication skills, creativity, and a passion for advancing science through MedTech.

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.



Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.