Senior Clinical Research Coordinator — Oncology Trials

University of Minnesota; Minneapolis (MN); On-site; USD 65,000 - 77,000; Full time

Benefits offered by this job

Competitive wages

Regents Tuition Benefit Program

Health, dental, vision plans

PSLF opportunity

Job summary

The University of Minnesota seeks a Clinical Research Coordinator III to manage clinical research data collection, study documentation, and protocol procedures in collaboration with the PI and team.

The role requires adherence to GCP, IRB, FDA CFR, and ICH guidelines, with emphasis on data integrity and patient safety. Requires strong attention to detail and independent work ethic, with mentoring duties for CRCs I/II.

Qualifications

• BA/BS with 4+ years of experience or an advanced degree and 2 years of experience, or 8 years of relevant education and 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 the required timeline in accordance with institutional requirements.
• Ensures protocol adherence by communicating and ensuring study parameters are executed according to protocol.
• Oversees visits with outside sponsors, including site initiation visits, interim monitoring visits, and closeout visits.
• Collaborates with PI and study team to enroll study participants, execute study-required procedures, and maintain accurate source documentation.
• Maintains a processing and tracking system for protocol-required biospecimens, data, and procedures.
• Works as a member of the study team with positive and timely written and verbal communication, including sharing information up, down, and laterally.
• Troubleshoots problems in the development and implementation of protocol procedures.
• Coordinates with Investigational Drug Services (IDS), BioNet, clinical staff, and other bodies across campus to deliver drug, collect biospecimens, and execute the study visits according to protocol.

Skills

Attention to detail

Organizational skills

Independent work

Team collaboration

Microsoft Office proficiency

Education

BA/BS in health sciences or related field

Advanced degree in healthcare or research

Clinical Research Coordinator certification or equivalent

Tools

Epic

OnCore

CTMS

Job description

The University of Minnesota seeks a Clinical Research Coordinator III to manage clinical research data collection, study documentation, and protocol procedures in collaboration with the PI and team.

The role requires adherence to GCP, IRB, FDA CFR, and ICH guidelines, with emphasis on data integrity and patient safety. Requires strong attention to detail and independent work ethic, with mentoring duties for CRCs I/II.