Clinical Research Coordinator OR RN Research Coordinator.

Avera Research Oncology

Worker Type:

Regular

Work Shift:

Day Shift (United States of America)

Pay Range:

The pay range for this position is listed below. Actual pay rate dependent upon experience.

$24.00 - $46.25

Position Highlights

For this position, we will hire either a Clinical Research Coordinator or a RN Research Coordinator.

• Clinical Research Coordinator Pay Range: $24.00 - $36.50

• RN Research Coordinator Pay Range: $31.00 - $46.25

Clinical Research Coordinator Brief Overview

Responsible for coordinating assigned clinical research studies by performing diverse clinical, regulatory, and clerical responsibilities requiring analysis, judgment, and knowledge of clinical research. Facilitates clinical research studies with participants, staff, investigators, and sponsoring organizations. The Coordinator works with patients and their families, beginning with evaluation and continuing through all required treatment phases of the clinical trial, in a compassionate and professional manner in order to achieve excellence in quality patient care and fulfill protocol requirements.

Required Education, License/Certification, or Work Experience:

• Bachelor's Health and science field

• 1-3 years clinical research, laboratory, or oncology or hematology

RN Research Coordinator Brief Overview

Responsible for coordinating assigned clinical research studies by performing diverse clinical, regulatory, and clerical responsibilities requiring analysis, judgment, and knowledge of clinical research. Facilitates clinical research studies with participants, staff, investigators, and sponsoring organizations. The coordinator works with patients and their families, beginning with evaluation and continuing through all required treatment phases of the clinical trial, in a compassionate and professional manner in order to achieve excellence in quality patient care and fulfill protocol requirements.

Required Education, License/Certification, or Work Experience:

• Registered Nurse (RN) - Board of Nursing An active license in the state of practice Upon Hire

• 1-3 years research or oncology, transplant or hematology

You Belong at Avera

Be part of a multidisciplinary team built with compassion and the goal of Moving Health Forward for you and our patients. Work where you matter.

A Brief Overview

Responsible for coordinating assigned clinical research studies by performing diverse clinical, regulatory, and clerical responsibilities requiring analysis, judgment, and knowledge of clinical research. Facilitates clinical research studies with participants, staff, investigators, and sponsoring organizations. The Coordinator works with patients and their families, beginning with evaluation and continuing through all required treatment phases of the clinical trial, in a compassionate and professional manner in order to achieve excellence in quality patient care and fulfill protocol requirements.

What you will do

• Coordinates multiple complex protocols at a time, for all drug development phases of the cancer research treatment in working with providers, patients and their family, as well as ancillary departments as needed for patient care coordination.
• Assures all appropriate information in patient cancer treatment status is communicated accordingly, and the research intervention is implemented.
• Collaborates with investigators, ancillary departments, study sponsors, internal and external monitors and auditors to facilitate compliance with the requirements of the research protocol with regards to good clinical research practice, FDA regulations, and policies that affect research at the institutional, state, federal and international level, while remaining cognizant of the needs of diverse patient populations.
• Utilizes multiple communication and research-specific education methods with research, clinical, and organizational staff, as well as patients and their significant others, to facilitate the effective conduct of clinical trials including the promotion and integrity of the clinical trial, and advocates for the safety and care of clinical trial patients.
• Develops and maintains respectful and trustworthy relationships with providers and their clinical staff, ancillary departments, and study sponsors to facilitate compliance with and successful accrual of eligible patients to clinical trials, all while ensuring proper use of and accountability