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Category: Nursing Professionals
Facility: IHA ClinSite
Department: Nursing
Schedule: Full Time
Hours: 40 hours
Job Details: RN (Registered Nurse)
1 Year (Minimum) Previous Experience (Required)
     The Clinical Research Coordinator II, implements moderate to highly complex clinical trials on an independent basis at ClinSite.  Serves as the interface between the Sponsor, ClinSite and the Principal Investigator (PI) by performing the following duties.
     Responsible for study start-up activities including: attending investigator meeting; initiating and planning the study kick off; tracking and receiving study supplies necessary for screening patients and completing electronic data capture and sponsor training.
     Accountable for overall recruitment for study. Also assists other staff with recruiting for study including data-mining, phone screening and generating reports.
     Prepares for and conducts patient visits, completes data entry, processes labs, and completes drug accountability, queries resolution and acts as a liaison between site and Sponsor/Contract Research Organization (CRO).
     Responsible for understanding clinical trial protocols and responsible for training appropriate staff on clinical trial protocol.
     Participates in new Clinical Research Coordinator training, continuing education for all staff and acts as a resource for Clinical Research Coordinator I’s. Assists management in driving recruitment and monthly revenue for site.
     Continues knowledge of industry news and assists management to keep ClinSite’s Standard Operating Procedures (SOPs) and processes up to date and in accordance with current industry standards.
     To perform the job successfully, an individual should demonstrate competencies in designated therapeutic areas. The ability to understand the potential impact of decisions on the scientific outcome of the study. Works well in group problem solving situation and  apply judgment to simple study specific issues.
     Responsible for end-to-end study coordination on simple to moderately complex studies. Operates within scope of clinical responsibilities and identifies when to include PI and/or supervisor.  


1. RN licensed to practice in Michigan

2. Minimum of three (3) years previous clinical experience. 

3. Ability to draw blood, process labs, record vital signs and perform ECGs.

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