Clinical Research Coordinator I — Drive Meaningful Trials

ThermoFisher Scientific; Richfield (MN); On-site; USD 36,000 - 40,000; Full time

Benefits offered by this job

Total Rewards package

Medical and dental plans

Vision plan

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Coordinator I to coordinate and manage clinical trials, ensuring protocol adherence, regulatory compliance, and timely data collection while supporting patient recruitment and documentation.

You will work with the clinical team to advance medical research, with trials conducted globally and a focus on quality and accuracy to improve health outcomes.

Qualifications

• Bachelor's degree in clinical/medical field or equivalent.
• BLS certification required.
• 0–2 years' experience in clinical research or similar role.

Responsibilities

• Coordinate clinical studies in line with FDA/GCP/ICH regulations.
• Provide medical care to patients with safety as priority.
• Perform study activities: informed consent, screening, protocol procedures (vitals, tests, ECGs).
• Handle phlebotomy and sample processing/shipping.
• Record patient data and test results per protocol.
• Maintain IP accountability logs where required.
• Report non-compliance to site staff.
• Ensure IRB approvals and ongoing requirements.

Skills

GCP knowledge

Clinical data collection

Documentation

Communication

English fluency

Education

Bachelor's degree in clinical/medical field

BLS certification

Tools

EHR systems

Job description

Thermo Fisher Scientific is seeking a Clinical Research Coordinator I to coordinate and manage clinical trials, ensuring protocol adherence, regulatory compliance, and timely data collection while supporting patient recruitment and documentation.

You will work with the clinical team to advance medical research, with trials conducted globally and a focus on quality and accuracy to improve health outcomes.