Clinical Research Coordinator II: Data-Driven Trials

University of Minnesota; Saint Paul (MN); On-site; USD 52,000 - 63,000; Full time

Benefits offered by this job

Paid holidays

Tuition benefits

Low-cost medical plans

HSA contributions

Retirement plans

PSLF opportunity

Job summary

The University of Minnesota – Masonic Cancer Center is seeking a Clinical Research Coordinator II to manage data collection, protocol procedures, and study documentation, ensuring GCP compliance and data integrity.

Responsibilities include coordinating with PI and sponsors, maintaining source documentation, and overseeing biospecimen processing, with a focus on accurate, timely study conduct and regulatory adherence.

Qualifications

• BA/BS with at least 2 years of experience or 6 years of relevant education & healthcare or research experience
• Excellent attention to detail and organizational skills
• Ability to work independently, as part of a team, and with changing priorities
• Computer proficiency in a PC environment including Microsoft Office products
• Ability to sit for extended periods of time

Responsibilities

• Interprets protocols and creates source documents needed for clinical research study
• Identifies and reports protocol deviations within required timelines
• Ensures protocol adherence by communicating and ensuring study parameters are executed according to protocol
• Oversees visits with outside sponsors, including site initiation, monitoring and closeout visits
• Collaborates with PI and study team to enroll participants and maintain accurate source documentation
• Maintains a processing and tracking system for biospecimens, data, and procedures
• Coordinates with IDS, BioNet, clinical staff, and others to deliver drug and collect biospecimens
• Troubleshoots problems in protocol procedures

Skills

Attention to detail

Organizational skills

Independent work

Team collaboration

Microsoft Office

Education

BA/BS + 2y expr

Healthcare/research education

Tools

CTMS

Epic

Oncore

Job description

The University of Minnesota – Masonic Cancer Center is seeking a Clinical Research Coordinator II to manage data collection, protocol procedures, and study documentation, ensuring GCP compliance and data integrity.

Responsibilities include coordinating with PI and sponsors, maintaining source documentation, and overseeing biospecimen processing, with a focus on accurate, timely study conduct and regulatory adherence.