Clinical Research Coordinator, RN

Healthcare Support Staffing; Appleton (WI); On-site; USD 65,000 - 85,000; Full time

Job summary

A healthcare staffing agency is seeking a Clinical Research Coordinator in Appleton, Wisconsin. The ideal candidate will have 1-2 years of experience in a hospital or clinic, with certifications such as SOCRA or CCRP. Responsibilities include ensuring compliance with federal regulations, training research teams, and assisting with coordinated care for research patients. This role offers day shifts, with a 13-week assignment and the potential for hire afterwards.

Qualifications

• 1-2 years of Hospital or Clinic experience required.
• SOCRA or CCRP certification is mandatory.
• In-depth knowledge of federal regulations.
• Familiarity with GCP, HIPAA, and IRB regulations.

Responsibilities

• Function independently as a clinical research coordinator.
• Promote ethical clinical practices.
• Assist clinical research nurse in coordinating research patients.
• Maintain compliance with protocol and regulatory requirements.

Skills

Clinical research experience

Knowledge of federal regulations

GCP

HIPAA compliance

IRB regulations knowledge

Education

Bachelor's degree in health sciences

SOCRA or CCRP Certification

Job description

Job Description

• Oncology clinical research coordinator will function independently and interdependently in collaboration with the clinical research nurse and other health care providers to promote ethical clinical practices in the conduct of clinical investigations.
• The coordinator must demonstrate an in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials to ensure human subject protection, compliance with protocol and regulatory requirements and the thorough collection, recording and maintenance of data and source documentation.
• Completion of regulatory and compliance forms, tracking of research training for participating specialty clinics, and maintenance of other research projects within the system, EPIC research module, and tracking and shipment of all protocol related submissions.
• This role functions to assist the clinical research nurse with care coordination of research patients and the research team in coordinating and facilitating the activities of all participants.

Qualifications

• Minimum of 1-2 years of Hospital or Clinic experience required.
• Society of Clinical Research Associate Certification (SOCRA) or Certified Clinical Research Professional Certification (CCRP).
• Bachelors degree in health sciences preferred.
• Clinical research experience, familiarity with federal regulations, GCP, HIPAA and IRB regulations.

Additional Information

• Shifts: M-F / day time shift
• Length of Assignment: 13 weeks then Right to Hire