Clinical Research Nurse Coordinator

The Cancer & Hematology Centers•Grand Rapids, MI

3d•Onsite

About The Position

General Summary The Clinical Research Nurse Coordinator, in collaboration with the physician Principal Investigator, ensures the integrity and quality of clinical trials are maintained while working closely with the physician and the study participant to ensure both the needs of the patient and the study are fulfilled. This position is primarily responsible for patient education regarding the study and the accurate completion of patient visit procedures according to protocols.

Requirements

Bachelor of Science in Nursing
Two years of work experience in Oncology/Hematology, or similar
Active Nursing license in State of Michigan
CPR/BCLS
Excellent assessment and record keeping skills with an ability to work efficiently in fast paced environment.

Nice To Haves

Previous research experience preferred
Oncology Certified Nurse - Preferred
Working knowledge of computer applications, including electronic medical records and Microsoft Applications.
Excellent written and verbal communication skills
Ability to review detailed data and make prompt judgments based on that data.
Able to multi-task efficiently

Responsibilities

Follows the patient from referral through treatment, discharge, and follow-up while providing patient and family education.
Coordinates and organizes patient care including recruitment (10%), screening (25%), scheduling (15%), consenting (15%), conducting visits (20%), and collecting various assessments such as adverse event information and questionnaires (15%).
Serve as a liaison for enrolled clinical trial patients to address patient concerns while on study and help facilitate study treatment assessments to include, attending patient doctor visits, capturing and reporting adverse events, coordinating logistical requirements with physicians (i.e. radiology tests), and educating nursing staff in protocol requirements.
Conducts all study activities in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP).
Performs the informed consent process following GCP.
Maintains and assists in the development of clinical records and study source documentation.
Prepares for study monitoring visits.
Assists with correcting findings and queries and management of investigational products (IP)
Participates in study meetings and conference calls.
Uses the electronic medical record (EMR) as needed, including reporting procedure results.
Function as a team member by expanding his/her responsibilities as directed by management to facilitate optimal workflow within all Cancer and Hematology Centers.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.