Senior Clinical Research Associate

About the Role

Join Bright Research as a Senior Clinical Research Associate
. This in‑person position is located downtown Minneapolis.

Are you curious and passionate about Med Tech and emerging devices and therapies? If you have strong communication skills, creativity, resilience and a positive attitude, we would love to hear from you!

• Collect, review, and maintain essential clinical trial documents throughout the study lifecycle using the electronic Trial Master File (eTMF), ensuring quality and regulatory compliance.
• Schedule, prepare for, and conduct site visits (SIVs, IMVs, COVs), including writing visit reports, resolving queries, and ensuring adherence to the monitoring plan and protocols.
• Monitor site activities for compliance with protocols and regulations; identify and elevate site performance or quality issues and support their resolution.
• Collaborate with site staff and study teams, lead site personnel training, and provide feedback on protocol conduct, documentation, and recruitment.
• Contribute to the development of monitoring tools and training materials, perform quality control checks on study documents, and assist with other clinical operations projects as needed.

• Bachelor’s or master’s degree in a scientific or engineering field, or equivalent work experience.
• At least 3 years of experience in clinical study monitoring, site management, and data management, and/or research experience with a proficient understanding of clinical trials methodology and terminology.
• Salary range: $70,000 - $100,000.

• Paid parking.
• Health insurance.
• Paid parental leave.
• 401(k) match.
• At least 10 paid company holidays.
• On‑site gym membership.

• Seniority level:
  Mid‑Senior level.
• Employment type:
  
  Full‑time.
• Job function:
  Research, Analyst, and Information Technology.
• Industries:
  Research Services.