Clinical Research Nurse
About The Position
The Clinical Research Nurse, in addition to performing standard nursing duties, plays a critical role in the conduct of clinical studies by supporting, facilitating, and coordinating the daily clinical study activities under the direction of the Principal Investigator (PI). The Clinical Research Nurse works with the PI, department, sponsor, and institution to support and provide guidance on the administration, compliance, financial, required personnel and other aspects of clinical studies . The Clinical Research Nurse oversees investigational drug and/or device accountability. Requires a higher level of supervision by Lead/Manager, with expectation of continuous progress in learning/understanding of role. Responsible for clinical operations activities for assigned studies & participants Serves as single contact person for research participants, Investigators, clinic and ancillary staff, Sponsors, and CROs Responsible for data entry, data query resolution in clinical study database, as well as other study-specific system management for assigned studies Supports, facilitates, and coordinates daily clinical study activities in support of study conduct Supports PI, departmental, Sponsor, and CRO inquiries Prepares/maintains research records and files in concert with regulatory requirements and Institutional files Conducts informed consent Conducts screening and recruitment procedures The Schedule: Monday - Friday, Days
Requirements
- 2 years Applicable Experience
- Registered Nurse (MO)
- Multi-State - National Council of State Boards of Nursing (NURSYS)
- Registered Nurse (MO) - National Council of State Boards of Nursing (NURSYS)
- Bachelor's Degree
Responsibilities
- supporting, facilitating, and coordinating the daily clinical study activities under the direction of the Principal Investigator (PI)
- overseeing investigational drug and/or device accountability
- clinical operations activities for assigned studies & participants
- Serves as single contact person for research participants, Investigators, clinic and ancillary staff, Sponsors, and CROs
- data entry, data query resolution in clinical study database, as well as other study-specific system management for assigned studies
- Supports PI, departmental, Sponsor, and CRO inquiries
- Prepares/maintains research records and files in concert with regulatory requirements and Institutional files
- Conducts informed consent
- Conducts screening and recruitment procedures
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
1,001-5,000 employees
