Clinical Research Coordinator | Coborn Cancer Center

CentraCare•Saint Cloud, MN

2d•$22 - $34

About The Position

In this position you are responsible for regulatory activities within the research department that require an in-depth understanding of Federal, Sponsor, and Institutional Review Board (IRB) regulatory guidelines. Ensures all cancer research protocols are administered meeting regulatory and legal requirements. Functions as first contact person for questions and audits related to regulatory aspects of the cancer research program including audits by the Federal Government, Sponsor(s) and internal. Supports and implements patient safety and other safety practices as appropriate. Supports and demonstrates Family Centered Care principles when interacting with patients and their families and with co-workers.

Requirements

Associate degree or higher degree required or two years' experience in a science, research, health related or complex administrative setting required.
2 years Minimum of experience in clinical trial conduct preferred.
Working understanding of medical terminology and the ability to communicate with staff and leadership.
Strong organizational skills in addition to the ability to multitask and prioritize required.

Nice To Haves

Clinical Research Associate National Certification preferred.
Training and knowledge of clinical research activities and regulatory requirements preferred.

Responsibilities

responsible for regulatory activities within the research department
Ensures all cancer research protocols are administered meeting regulatory and legal requirements
Functions as first contact person for questions and audits related to regulatory aspects of the cancer research program including audits by the Federal Government, Sponsor(s) and internal
Supports and implements patient safety and other safety practices as appropriate
Supports and demonstrates Family Centered Care principles when interacting with patients and their families and with co-workers