Clinical Research Nurse-Senior
About The Position
Under limited supervision, the Clinical Research Nurse actively facilitates clinical research by administering and monitoring treatment or research protocols. The role coordinates and participates in studies conducted by principal investigators and handles complex activities involving recruitment, collection, compilation, documentation, and analysis of clinical research data. The nurse also assists in establishing guidelines for clinical data collection and study administration, and may lead or mentor lower-level team members. The position coordinates and manages clinical research projects according to study protocols, including assessment, planning, evaluation, and intervention to support participant well-being. It reviews prospective studies for feasibility, supports study initiation, and helps plan and design source documentation. The role prepares and maintains regulatory documents and submissions, ensures compliance with applicable regulations and institutional and research-organization policies, and monitors study close-out and record retention. Other duties may be assigned.
Requirements
- Associate's degree required.
- Ability to communicate and liaise with research participants, research team members, and relevant partners and stakeholders.
- Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
- Demonstrated ability to monitor important and complex projects concurrently.
- Ability to work independently with minimal supervision.
Responsibilities
- Screen, recruit, and consent study participants; verify eligibility and complete screening procedures.
- Schedule and conduct study visits; collect and process data; complete case report forms and electronic data entry; and maintain study-subject data.
- Instruct and counsel patients on research procedures, administer treatment procedures, monitor patients during procedures, and record and analyze data.
- Evaluate patients and collaborate with physicians to ensure a goal-specific plan of care.
- Review potential research studies for feasibility.
- Prepare and maintain regulatory documents and submit materials for new studies, amendments, annual progress reports, and final reports to relevant internal and external agencies.
- Ensure compliance with federal and local regulations and applicable institutional and research-organization policies.
- Monitor study close-out and ensure records are retained for the appropriate period.
- Review new protocol goals and requirements, plan and design source documentation, and coordinate study initiation.
- Coordinate and manage clinical research projects for the principal investigator according to study protocols, including assessment, planning, evaluation, and intervention for participant well-being.
- May lead or mentor lower-level team members.
- Perform other duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Associate degree
